Analysis | Hit | start | end | length | Note | Hit coverage | Hit length | Hit pident | Hit pcons | eValue | Hit description |
blastp_kegg | bfu:BC1G_10347 | 1 | 522 | 522 | Gaps:26 | 87.63 | 566 | 85.69 | 0.00 | 0.0 | hypothetical protein K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
ssl:SS1G_02271 | 137 | 522 | 386 | n/a | 87.53 | 441 | 77.98 | 1.04 | 1e-170 | hypothetical protein K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
pno:SNOG_06430 | 1 | 520 | 520 | Gaps:36 | 87.67 | 584 | 55.27 | 10.35 | 1e-143 | hypothetical protein K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
act:ACLA_083160 | 1 | 520 | 520 | Gaps:39 | 87.61 | 565 | 52.32 | 9.29 | 1e-128 | protein kinase putative K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
fgr:FG08631.1 | 1 | 519 | 519 | Gaps:76 | 86.40 | 522 | 56.98 | 10.42 | 1e-125 | hypothetical protein K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
tml:GSTUM_00007000001 | 1 | 520 | 520 | Gaps:73 | 86.56 | 521 | 54.10 | 12.42 | 1e-118 | hypothetical protein K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
ang:An11g07450 | 40 | 520 | 481 | Gaps:46 | 91.77 | 498 | 52.08 | 9.63 | 1e-115 | hypothetical protein K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
nfi:NFIA_054920 | 1 | 520 | 520 | Gaps:29 | 66.31 | 567 | 64.10 | 9.04 | 1e-105 | protein kinase putative K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
afm:AFUA_6G09240 | 1 | 520 | 520 | Gaps:29 | 66.31 | 567 | 63.83 | 9.04 | 1e-105 | protein kinase K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
ncr:NCU07062 | 1 | 519 | 519 | Gaps:45 | 75.70 | 568 | 57.67 | 9.30 | 1e-105 | hypothetical protein K08793 serine/threonine kinase 32 [EC:2.7.11.1] |
blastp_uniprot_sprot | sp|Q8MYF1|Y2070_DICDI | 1 | 259 | 259 | Gaps:35 | 51.75 | 456 | 40.25 | 23.31 | 6e-44 | Probable serine/threonine-protein kinase DDB_G0277449 OS Dictyostelium discoideum GN DDB_G0277449 PE 3 SV 1 |
sp|Q8WU08|ST32A_HUMAN | 1 | 263 | 263 | Gaps:36 | 60.35 | 396 | 40.17 | 21.76 | 4e-42 | Serine/threonine-protein kinase 32A OS Homo sapiens GN STK32A PE 2 SV 2 |
sp|Q9WUT3|KS6A2_MOUSE | 1 | 252 | 252 | Gaps:47 | 55.80 | 733 | 37.41 | 18.34 | 8e-42 | Ribosomal protein S6 kinase alpha-2 OS Mus musculus GN Rps6ka2 PE 2 SV 1 |
sp|O74426|PPK33_SCHPO | 1 | 263 | 263 | Gaps:45 | 75.15 | 338 | 37.40 | 16.54 | 2e-41 | Serine/threonine-protein kinase ppk33 OS Schizosaccharomyces pombe GN ppk33 PE 2 SV 1 |
sp|Q15349|KS6A2_HUMAN | 1 | 252 | 252 | Gaps:47 | 55.39 | 733 | 36.95 | 17.98 | 7e-41 | Ribosomal protein S6 kinase alpha-2 OS Homo sapiens GN RPS6KA2 PE 1 SV 2 |
sp|Q8BGW6|ST32A_MOUSE | 1 | 263 | 263 | Gaps:40 | 60.05 | 398 | 39.75 | 21.76 | 8e-41 | Serine/threonine-protein kinase 32A OS Mus musculus GN Stk32a PE 2 SV 1 |
sp|P18652|KS6AA_CHICK | 1 | 252 | 252 | Gaps:43 | 53.99 | 752 | 37.44 | 17.24 | 8e-40 | Ribosomal protein S6 kinase 2 alpha OS Gallus gallus GN RPS6KA PE 2 SV 1 |
sp|P28178|PK2_DICDI | 1 | 251 | 251 | Gaps:30 | 46.56 | 479 | 39.91 | 20.18 | 1e-39 | Protein kinase 2 OS Dictyostelium discoideum GN pkgB PE 1 SV 2 |
sp|P83099|KPC4_DROME | 6 | 251 | 246 | Gaps:37 | 32.94 | 671 | 42.99 | 17.65 | 3e-39 | Putative protein kinase C delta type homolog OS Drosophila melanogaster GN Pkcdelta PE 1 SV 3 |
sp|Q9UK32|KS6A6_HUMAN | 1 | 263 | 263 | Gaps:37 | 48.99 | 745 | 38.08 | 17.81 | 3e-39 | Ribosomal protein S6 kinase alpha-6 OS Homo sapiens GN RPS6KA6 PE 1 SV 1 |
blastp_pdb | 3g51_A | 1 | 253 | 253 | Gaps:33 | 70.15 | 325 | 39.91 | 18.42 | 1e-39 | mol:protein length:325 Ribosomal protein S6 kinase alpha-3 |
2z7s_A | 1 | 252 | 252 | Gaps:33 | 70.72 | 321 | 39.65 | 18.94 | 6e-39 | mol:protein length:321 Ribosomal protein S6 kinase alpha-1 |
2z7r_A | 1 | 252 | 252 | Gaps:33 | 70.72 | 321 | 39.65 | 18.94 | 6e-39 | mol:protein length:321 Ribosomal protein S6 kinase alpha-1 |
2z7q_A | 1 | 252 | 252 | Gaps:33 | 70.72 | 321 | 39.65 | 18.94 | 6e-39 | mol:protein length:321 Ribosomal protein S6 kinase alpha-1 |
1zrz_A | 6 | 262 | 257 | Gaps:47 | 67.58 | 364 | 37.80 | 19.92 | 2e-36 | mol:protein length:364 Protein kinase C iota |
3a8x_B | 6 | 262 | 257 | Gaps:47 | 71.30 | 345 | 37.80 | 19.92 | 3e-36 | mol:protein length:345 Protein kinase C iota type |
3a8x_A | 6 | 262 | 257 | Gaps:47 | 71.30 | 345 | 37.80 | 19.92 | 3e-36 | mol:protein length:345 Protein kinase C iota type |
3a8w_B | 6 | 262 | 257 | Gaps:47 | 71.30 | 345 | 37.80 | 19.92 | 3e-36 | mol:protein length:345 Protein kinase C iota type |
3a8w_A | 6 | 262 | 257 | Gaps:47 | 71.30 | 345 | 37.80 | 19.92 | 3e-36 | mol:protein length:345 Protein kinase C iota type |
3iw4_C | 50 | 262 | 213 | Gaps:10 | 60.28 | 360 | 37.79 | 19.35 | 2e-35 | mol:protein length:360 Protein kinase C alpha type |
rpsblast_cdd | gnl|CDD|173669 | 1 | 232 | 232 | Gaps:28 | 79.84 | 258 | 50.00 | 16.50 | 2e-78 | cd05578 STKc_Yank1 Catalytic domain of the Protein Serine/Threonine Kinase Yank1. Serine/Threonine Kinases (STKs) Yank1 or STK32A subfamily catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The Yank1 subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs protein tyrosine kinases RIO kinases aminoglycoside phosphotransferase choline kinase and phosphoinositide 3-kinase. This subfamily contains uncharacterized STKs with similarity to the human protein designated Yank1 or STK32A. |
gnl|CDD|173660 | 1 | 232 | 232 | Gaps:35 | 82.00 | 250 | 45.37 | 17.56 | 3e-59 | cd05123 STKc_AGC Catalytic domain of AGC family Protein Serine/Threonine Kinases. Serine/Threonine Kinases (STKs) AGC (Protein Kinases A G and C) family catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The AGC family is part of a larger superfamily that includes the catalytic domains of other protein STKs protein tyrosine kinases RIO kinases aminoglycoside phosphotransferase choline kinase and Phosphoinositide 3-Kinase (PI3K). Members of this family include cAMP-dependent Protein Kinase (PKA) cGMP-dependent Protein Kinase (PKG) Protein Kinase C (PKC) Protein Kinase B (PKB) G protein-coupled Receptor Kinase (GRK) Serum- and Glucocorticoid-induced Kinase (SGK) and 70 kDa ribosomal Protein S6 Kinase (p70S6K or S6K) among others. AGC kinases share an activation mechanism based on the phosphorylation of up to three sites: the activation loop (A-loop) the hydrophobic motif (HM) and the turn motif. Phosphorylation at the A-loop is required of most AGC kinases which results in a disorder-to-order transition of the A-loop. The ordered conformation results in the access of substrates and ATP to the active site. A subset of AGC kinases with C-terminal extensions containing the HM also requires phosphorylation at this site. Phosphorylation at the HM allows the C-terminal extension to form an ordered structure that packs into the hydrophobic pocket of the catalytic domain which then reconfigures the kinase into an active bi-lobed state. In addition growth factor-activated AGC kinases such as PKB p70S6K RSK MSK PKC and SGK require phosphorylation at the turn motif (also called tail or zipper site) located N-terminal to the HM at the C-terminal extension. AGC kinases regulate many cellular processes including division growth survival metabolism motility and differentiation. Many are implicated in the development of various human diseases. |
gnl|CDD|128516 | 1 | 221 | 221 | Gaps:28 | 80.74 | 244 | 40.61 | 15.23 | 1e-56 | smart00220 S_TKc Serine/Threonine protein kinases catalytic domain. Phosphotransferases. Serine or threonine-specific kinase subfamily. |
gnl|CDD|173683 | 7 | 274 | 268 | Gaps:34 | 75.32 | 316 | 41.18 | 17.23 | 4e-50 | cd05592 STKc_nPKC_theta_delta Catalytic domain of the Protein Serine/Threonine Kinases Novel Protein Kinase C theta and delta. Serine/Threonine Kinases (STKs) Novel Protein Kinase C (nPKC) theta and delta-like isoforms catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The nPKC subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs protein tyrosine kinases RIO kinases aminoglycoside phosphotransferase choline kinase and phosphoinositide 3-kinase. PKCs are classified into three groups (classical atypical and novel) depending on their mode of activation and the structural characteristics of their regulatory domain. nPKCs are calcium-independent but require DAG (1 2-diacylglycerol) and phosphatidylserine (PS) for activity. There are four nPKC isoforms delta epsilon eta and theta. PKC-theta is selectively expressed in T-cells and plays an important and non-redundant role in several aspects of T-cell biology. PKC-delta plays a role in cell cycle regulation and programmed cell death in many cell types. |
gnl|CDD|173661 | 6 | 269 | 264 | Gaps:41 | 76.42 | 318 | 40.74 | 18.93 | 2e-47 | cd05570 STKc_PKC Catalytic domain of the Protein Serine/Threonine Kinase Protein Kinase C. Serine/Threonine Kinases (STKs) Protein Kinase C (PKC) subfamily catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The PKC subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs protein tyrosine kinases RIO kinases aminoglycoside phosphotransferase choline kinase and phosphoinositide 3-kinase. PKCs are classified into three groups (classical atypical and novel) depending on their mode of activation and the structural characteristics of their regulatory domain. PKCs undergo three phosphorylations in order to take mature forms. In addition classical PKCs depend on calcium DAG (1 2-diacylglycerol) and in most cases phosphatidylserine (PS) for activation. Novel PKCs are calcium-independent but require DAG and PS for activity while atypical PKCs only require PS. PKCs phosphorylate and modify the activities of a wide variety of cellular proteins including receptors enzymes cytoskeletal proteins transcription factors and other kinases. They play a central role in signal transduction pathways that regulate cell migration and polarity proliferation differentiation and apoptosis. Also included in this subfamily are the PKC-like proteins called PKNs. |
gnl|CDD|143851 | 1 | 217 | 217 | Gaps:33 | 76.15 | 260 | 38.38 | 14.65 | 1e-44 | pfam00069 Pkinase Protein kinase domain. |
gnl|CDD|173671 | 1 | 260 | 260 | Gaps:40 | 81.38 | 290 | 37.71 | 19.49 | 1e-44 | cd05580 STKc_PKA Catalytic domain of the Protein Serine/Threonine Kinase cAMP-dependent protein kinase. Serine/Threonine Kinases (STKs) cAMP-dependent protein kinase (PKA) subfamily catalytic (c) subunit. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The PKA subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs protein tyrosine kinases RIO kinases aminoglycoside phosphotransferase choline kinase and phosphoinositide 3-kinase (PI3K). This subfamily is composed of the cAMP-dependent proteins kinases PKA and PRKX. The inactive PKA holoenzyme is a heterotetramer composed of two phosphorylated and active catalytic (C) subunits with a dimer of regulatory (R) subunits. Activation is achieved through the binding of the important second messenger cAMP to the R subunits which leads to the dissociation of PKA into the R dimer and two active C subunits. PKA is present ubiquitously in cells and interacts with many different downstream targets. It plays a role in the regulation of diverse processes such as growth development memory metabolism gene expression immunity and lipolysis. |
gnl|CDD|173673 | 1 | 265 | 265 | Gaps:37 | 75.47 | 318 | 40.83 | 19.17 | 3e-44 | cd05582 STKc_RSK_N N-terminal catalytic domain of the Protein Serine/Threonine Kinase 90 kDa ribosomal protein S6 kinase. Serine/Threonine Kinases (STKs) 90 kDa ribosomal protein S6 kinase (RSK) subfamily N-terminal catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The RSK subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs protein tyrosine kinases RIO kinases aminoglycoside phosphotransferase choline kinase and phosphoinositide 3-kinase. RSKs contain an N-terminal kinase domain (NTD) from the AGC family and a C-terminal kinase domain (CTD) from the CAMK family. They are activated by signaling inputs from extracellular regulated kinase (ERK) and phosphoinositide dependent kinase 1 (PDK1). ERK phosphorylates and activates the CTD of RSK serving as a docking site for PDK1 which phosphorylates and activates the NTD which in turn phosphorylates all known RSK substrates. RSKs act as downstream effectors of mitogen-activated protein kinase (MAPK) and play key roles in mitogen-activated cell growth differentiation and survival. Mammals possess four RSK isoforms (RSK1-4) from distinct genes. RSK proteins are also referred to as MAP kinase-activated protein kinases (MAPKAPKs) p90-RSKs or p90S6Ks. |
gnl|CDD|173674 | 1 | 251 | 251 | Gaps:39 | 80.56 | 288 | 39.66 | 23.28 | 3e-44 | cd05583 STKc_MSK_N N-terminal catalytic domain of the Protein Serine/Threonine Kinase Mitogen and stress-activated kinase. Serine/Threonine Kinases (STKs) Mitogen and stress-activated kinase (MSK) subfamily N-terminal catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The MSK subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs protein tyrosine kinases RIO kinases aminoglycoside phosphotransferase choline kinase and phosphoinositide 3-kinase. MSKs contain an N-terminal kinase domain (NTD) from the AGC family and a C-terminal kinase domain (CTD) from the CAMK family similar to 90 kDa ribosomal protein S6 kinases (RSKs). MSKs are activated by two major signaling cascades the Ras-MAPK and p38 stress kinase pathways in response to various stimuli such as growth factors hormones neurotransmitters cellular stress and pro-inflammatory cytokines. This triggers phosphorylation in the activation loop (A-loop) of the CTD of MSK. The active CTD phosphorylates the hydrophobic motif (HM) in the C-terminal extension of NTD which facilitates the phosphorylation of the A-loop and activates the NTD which in turn phosphorylates downstream targets. MSKs are predominantly nuclear proteins. They are widely expressed in many tissues including heart brain lung liver kidney and pancreas. There are two isoforms of MSK called MSK1 and MSK2. |
gnl|CDD|173664 | 6 | 275 | 270 | Gaps:72 | 77.71 | 350 | 41.18 | 12.13 | 4e-44 | cd05573 STKc_ROCK_NDR_like Catalytic domain of ROCK- and NDR kinase-like Protein Serine/Threonine Kinases. Serine/Threonine Kinases (STKs) Rho-associated coiled-coil containing protein kinase (ROCK) and Nuclear Dbf2-Related (NDR)-like kinase subfamily catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The ROCK- and NDR-like subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs protein tyrosine kinases RIO kinases aminoglycoside phosphotransferase choline kinase and phosphoinositide 3-kinase. Members of this subfamily include ROCK and ROCK-like proteins such as DMPK MRCK and CRIK as well as NDR and NDR-like proteins such as LATS CBK1 and Sid2p. ROCK and CRIK are effectors of the small GTPase Rho while MRCK is an effector of the small GTPase Cdc42. NDR and NDR-like kinases contain an N-terminal regulatory (NTR) domain and an insert within the catalytic domain that contains an auto-inhibitory sequence. Proteins in this subfamily are involved in regulating many cellular functions including contraction motility division proliferation apoptosis morphogenesis and cytokinesis. |
rpsblast_kog | gnl|CDD|35818 | 1 | 274 | 274 | Gaps:33 | 69.75 | 357 | 36.95 | 18.07 | 5e-60 | KOG0598 KOG0598 KOG0598 Ribosomal protein S6 kinase and related proteins [General function prediction only Signal transduction mechanisms]. |
gnl|CDD|35913 | 6 | 280 | 275 | Gaps:33 | 35.73 | 694 | 35.89 | 18.15 | 8e-49 | KOG0694 KOG0694 KOG0694 Serine/threonine protein kinase [Signal transduction mechanisms]. |
gnl|CDD|36204 | 1 | 266 | 266 | Gaps:32 | 41.62 | 591 | 32.52 | 21.54 | 1e-41 | KOG0986 KOG0986 KOG0986 G protein-coupled receptor kinase [Signal transduction mechanisms]. |
gnl|CDD|35915 | 50 | 262 | 213 | Gaps:11 | 31.92 | 683 | 38.53 | 17.89 | 4e-41 | KOG0696 KOG0696 KOG0696 Serine/threonine protein kinase [Signal transduction mechanisms]. |
gnl|CDD|35836 | 1 | 289 | 289 | Gaps:47 | 72.68 | 355 | 34.88 | 20.54 | 2e-40 | KOG0616 KOG0616 KOG0616 cAMP-dependent protein kinase catalytic subunit (PKA) [Signal transduction mechanisms]. |
gnl|CDD|35914 | 50 | 269 | 220 | Gaps:22 | 39.46 | 593 | 36.75 | 19.66 | 8e-39 | KOG0695 KOG0695 KOG0695 Serine/threonine protein kinase [Signal transduction mechanisms]. |
gnl|CDD|35825 | 6 | 280 | 275 | Gaps:94 | 54.36 | 550 | 31.77 | 15.05 | 2e-38 | KOG0605 KOG0605 KOG0605 NDR and related serine/threonine kinases [General function prediction only]. |
gnl|CDD|35832 | 2 | 263 | 262 | Gaps:44 | 18.68 | 1317 | 37.40 | 14.63 | 1e-37 | KOG0612 KOG0612 KOG0612 Rho-associated coiled-coil containing protein kinase [Signal transduction mechanisms]. |
gnl|CDD|35909 | 1 | 251 | 251 | Gaps:41 | 43.80 | 516 | 38.05 | 20.35 | 7e-37 | KOG0690 KOG0690 KOG0690 Serine/threonine protein kinase [Signal transduction mechanisms]. |
gnl|CDD|35812 | 6 | 292 | 287 | Gaps:49 | 44.37 | 604 | 31.34 | 16.04 | 1e-29 | KOG0592 KOG0592 KOG0592 3-phosphoinositide-dependent protein kinase (PDK1) [Signal transduction mechanisms]. |