Analysis | Hit | start | end | length | Note | Hit coverage | Hit length | Hit pident | Hit pcons | eValue | Hit description |
blastp_kegg | bfu:BC1G_07743 | 293 | 684 | 392 | n/a | 97.03 | 404 | 80.10 | 0.00 | 1e-175 | hypothetical protein |
bfu:BC1G_07742 | 1 | 218 | 218 | n/a | 99.09 | 220 | 98.62 | 0.46 | 1e-125 | hypothetical protein |
ssl:SS1G_07922 | 11 | 276 | 266 | Gaps:25 | 52.01 | 498 | 59.46 | 13.90 | 7e-77 | hypothetical protein |
ncr:NCU05722 | 33 | 376 | 344 | Gaps:74 | 61.30 | 522 | 29.06 | 19.06 | 5e-14 | hypothetical protein |
bfu:BC1G_02418 | 9 | 286 | 278 | Gaps:55 | 52.58 | 523 | 30.18 | 18.55 | 1e-13 | hypothetical protein |
ssl:SS1G_09709 | 28 | 224 | 197 | Gaps:40 | 20.85 | 820 | 31.58 | 22.22 | 4e-12 | hypothetical protein |
mgr:MGG_08709 | 33 | 380 | 348 | Gaps:75 | 45.94 | 764 | 28.77 | 18.23 | 1e-11 | MG08709.4 hypothetical protein |
ctp:CTRG_01934 | 143 | 386 | 244 | Gaps:39 | 47.28 | 459 | 30.88 | 20.74 | 7e-11 | similar to protein-serine/threonine kinase K08857 NIMA (never in mitosis gene a)-related kinase [EC:2.7.11.1] |
clu:CLUG_05229 | 143 | 387 | 245 | Gaps:50 | 39.10 | 555 | 33.64 | 17.51 | 1e-09 | hypothetical protein K08857 NIMA (never in mitosis gene a)-related kinase [EC:2.7.11.1] |
pgu:PGUG_02304 | 143 | 372 | 230 | Gaps:42 | 44.16 | 462 | 33.82 | 17.16 | 5e-09 | hypothetical protein K08857 NIMA (never in mitosis gene a)-related kinase [EC:2.7.11.1] |
blastp_uniprot_sprot | sp|Q86UE8|TLK2_HUMAN | 209 | 368 | 160 | Gaps:12 | 19.17 | 772 | 33.11 | 18.24 | 2e-09 | Serine/threonine-protein kinase tousled-like 2 OS Homo sapiens GN TLK2 PE 1 SV 2 |
sp|O55047|TLK2_MOUSE | 209 | 368 | 160 | Gaps:12 | 20.61 | 718 | 33.11 | 18.24 | 2e-09 | Serine/threonine-protein kinase tousled-like 2 OS Mus musculus GN Tlk2 PE 2 SV 2 |
sp|Q08CW1|TLK2_XENTR | 145 | 368 | 224 | Gaps:32 | 27.55 | 697 | 31.77 | 19.79 | 2e-09 | Serine/threonine-protein kinase tousled-like 2 OS Xenopus tropicalis GN tlk2 PE 2 SV 1 |
sp|Q8RXT4|NEK4_ARATH | 143 | 369 | 227 | Gaps:52 | 31.53 | 555 | 36.00 | 16.57 | 5e-09 | Serine/threonine-protein kinase Nek4 OS Arabidopsis thaliana GN NEK4 PE 2 SV 1 |
sp|Q9UKI8|TLK1_HUMAN | 209 | 368 | 160 | Gaps:13 | 19.19 | 766 | 31.97 | 17.69 | 2e-08 | Serine/threonine-protein kinase tousled-like 1 OS Homo sapiens GN TLK1 PE 1 SV 2 |
sp|Q8C0V0|TLK1_MOUSE | 209 | 368 | 160 | Gaps:13 | 19.19 | 766 | 31.97 | 17.69 | 2e-08 | Serine/threonine-protein kinase tousled-like 1 OS Mus musculus GN Tlk1 PE 2 SV 2 |
sp|Q9UIK4|DAPK2_HUMAN | 137 | 369 | 233 | Gaps:56 | 50.00 | 370 | 33.51 | 18.38 | 3e-08 | Death-associated protein kinase 2 OS Homo sapiens GN DAPK2 PE 1 SV 1 |
sp|Q8VDF3|DAPK2_MOUSE | 137 | 369 | 233 | Gaps:56 | 50.00 | 370 | 33.51 | 18.38 | 3e-08 | Death-associated protein kinase 2 OS Mus musculus GN Dapk2 PE 1 SV 1 |
sp|Q90ZY6|TLK1B_DANRE | 209 | 368 | 160 | Gaps:13 | 19.44 | 756 | 31.97 | 17.69 | 6e-08 | Serine/threonine-protein kinase tousled-like 1-B OS Danio rerio GN tlk1b PE 2 SV 1 |
sp|Q91XS8|ST17B_RAT | 134 | 382 | 249 | Gaps:57 | 54.99 | 371 | 32.84 | 18.63 | 1e-07 | Serine/threonine-protein kinase 17B OS Rattus norvegicus GN Stk17b PE 1 SV 1 |
blastp_pdb | 2a27_H | 137 | 369 | 233 | Gaps:56 | 57.63 | 321 | 33.51 | 18.38 | 3e-09 | mol:protein length:321 Death-associated protein kinase 2 |
2a27_G | 137 | 369 | 233 | Gaps:56 | 57.63 | 321 | 33.51 | 18.38 | 3e-09 | mol:protein length:321 Death-associated protein kinase 2 |
2a27_F | 137 | 369 | 233 | Gaps:56 | 57.63 | 321 | 33.51 | 18.38 | 3e-09 | mol:protein length:321 Death-associated protein kinase 2 |
2a27_E | 137 | 369 | 233 | Gaps:56 | 57.63 | 321 | 33.51 | 18.38 | 3e-09 | mol:protein length:321 Death-associated protein kinase 2 |
2a27_D | 137 | 369 | 233 | Gaps:56 | 57.63 | 321 | 33.51 | 18.38 | 3e-09 | mol:protein length:321 Death-associated protein kinase 2 |
2a27_C | 137 | 369 | 233 | Gaps:56 | 57.63 | 321 | 33.51 | 18.38 | 3e-09 | mol:protein length:321 Death-associated protein kinase 2 |
2a27_B | 137 | 369 | 233 | Gaps:56 | 57.63 | 321 | 33.51 | 18.38 | 3e-09 | mol:protein length:321 Death-associated protein kinase 2 |
2a27_A | 137 | 369 | 233 | Gaps:56 | 57.63 | 321 | 33.51 | 18.38 | 3e-09 | mol:protein length:321 Death-associated protein kinase 2 |
1zws_H | 135 | 369 | 235 | Gaps:56 | 64.93 | 288 | 33.16 | 18.72 | 3e-09 | mol:protein length:288 DAP-kinase related protein 1 |
1zws_G | 135 | 369 | 235 | Gaps:56 | 64.93 | 288 | 33.16 | 18.72 | 3e-09 | mol:protein length:288 DAP-kinase related protein 1 |
rpsblast_cdd | gnl|CDD|128516 | 143 | 369 | 227 | Gaps:53 | 72.13 | 244 | 31.25 | 14.77 | 6e-16 | smart00220 S_TKc Serine/Threonine protein kinases catalytic domain. Phosphotransferases. Serine or threonine-specific kinase subfamily. |
gnl|CDD|143851 | 32 | 369 | 338 | Gaps:110 | 96.92 | 260 | 29.76 | 18.25 | 1e-14 | pfam00069 Pkinase Protein kinase domain. |
gnl|CDD|173623 | 35 | 369 | 335 | Gaps:129 | 98.60 | 215 | 32.55 | 18.40 | 1e-14 | cd00180 PKc Catalytic domain of Protein Kinases. Protein Kinases (PKs) catalytic (c) domain. PKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine or tyrosine residues on protein substrates. The PK family is part of a larger superfamily that includes the catalytic domains of RIO kinases aminoglycoside phosphotransferase choline kinase phosphoinositide 3-kinase (PI3K) and actin-fragmin kinase. PKs make up a large family of serine/threonine kinases protein tyrosine kinases (PTKs) and dual-specificity PKs that phosphorylate both serine/threonine and tyrosine residues of target proteins. Majority of protein phosphorylation about 95% occurs on serine residues while only 1% occurs on tyrosine residues. Protein phosphorylation is a mechanism by which a wide variety of cellular proteins such as enzymes and membrane channels are reversibly regulated in response to certain stimuli. PKs often function as components of signal transduction pathways in which one kinase activates a second kinase which in turn may act on other kinases this sequential action transmits a signal from the cell surface to target proteins which results in cellular responses. The PK family is one of the largest known protein families with more than 100 homologous yeast enzymes and 550 human proteins. A fraction of PK family members are pseudokinases that lack crucial residues for catalytic activity. The mutiplicity of kinases allows for specific regulation according to substrate tissue distribution and cellular localization. PKs regulate many cellular processes including proliferation division differentiation motility survival metabolism cell-cycle progression cytoskeletal rearrangement immunity and neuronal functions. Many kinases are implicated in the development of various human diseases including different types of cancer. |
gnl|CDD|173724 | 28 | 369 | 342 | Gaps:103 | 98.08 | 260 | 29.02 | 19.61 | 6e-13 | cd06606 STKc_MAPKKK Catalytic domain of the Protein Serine/Threonine Kinase Mitogen-Activated Protein Kinase Kinase Kinase. Serine/threonine kinases (STKs) mitogen-activated protein kinase (MAPK) kinase kinase (MAPKKK) subfamily catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The MAPKKK 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. MAPKKKs (MKKKs or MAP3Ks) are also called MAP/ERK kinase kinases (MEKKs) in some cases. They phosphorylate and activate MAPK kinases (MAPKKs or MKKs or MAP2Ks) which in turn phosphorylate and activate MAPKs during signaling cascades that are important in mediating cellular responses to extracellular signals. This subfamily is composed of the Apoptosis Signal-regulating Kinases ASK1 (or MAPKKK5) and ASK2 (or MAPKKK6) MEKK1 MEKK2 MEKK3 MEKK4 as well as plant and fungal MAPKKKs. Also included in this subfamily are the cell division control proteins Schizosaccharomyces pombe Cdc7 and Saccharomyces cerevisiae Cdc15. |
gnl|CDD|30861 | 143 | 467 | 325 | Gaps:34 | 77.34 | 384 | 19.87 | 12.79 | 5e-11 | COG0515 SPS1 Serine/threonine protein kinase [General function prediction only / Signal transduction mechanisms / Transcription / DNA replication recombination and repair]. |
gnl|CDD|173757 | 123 | 369 | 247 | Gaps:52 | 75.09 | 265 | 32.66 | 14.57 | 2e-09 | cd08217 STKc_Nek2 Catalytic domain of the Protein Serine/Threonine Kinase Never In Mitosis gene A-related kinase 2. Serine/Threonine Kinases (STKs) Never In Mitosis gene A (NIMA)-related kinase 2 (Nek2) subfamily catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The Nek2 subfamily is one of a family of 11 different Neks (Nek1-11) that are involved in cell cycle control. The Nek 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. The Nek2 subfamily includes Aspergillus nidulans NIMA kinase the founding member of the Nek family which was identified in a screen for cell cycle mutants prevented from entering mitosis. NIMA is essential for mitotic entry and progression through mitosis and its degradation is essential for mitotic exit. NIMA is involved in nuclear membrane fission. Vertebrate Nek2 is a cell cycle-regulated STK localized in centrosomes and kinetochores that regulates centrosome splitting at the G2/M phase. It also interacts with other mitotic kinases such as Polo-like kinase 1 and may play a role in spindle checkpoint. An increase in the expression of the human NEK2 gene is strongly associated with the progression of non-Hodgkin lymphoma. |
gnl|CDD|173765 | 205 | 369 | 165 | Gaps:30 | 52.53 | 257 | 34.07 | 17.04 | 2e-09 | cd08225 STKc_Nek5 Catalytic domain of the Protein Serine/Threonine Kinase Never In Mitosis gene A-related kinase 5. Serine/Threonine Kinases (STKs) Never In Mitosis gene A (NIMA)-related kinase 5 (Nek5) subfamily catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The Nek5 subfamily is one of a family of 11 different Neks (Nek1-11). The Nek 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. Neks are involved in the regulation of downstream processes following the activation of Cdc2 and many of their functions are cell cycle-related. They play critical roles in microtubule dynamics during ciliogenesis and mitosis. The specific function of Nek5 is unknown. |
gnl|CDD|132957 | 143 | 369 | 227 | Gaps:51 | 69.70 | 264 | 30.43 | 15.22 | 2e-09 | cd06626 STKc_MEKK4 Catalytic domain of the Protein Serine/Threonine Kinase MAP/ERK kinase kinase 4. Serine/threonine kinases (STKs) MAP/ERK kinase kinase 4 (MEKK4) subfamily catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The MEKK4 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. MEKK4 is a mitogen-activated protein kinase (MAPK) kinase kinase (MAPKKK or MKKK or MAP3K) that phosphorylates and activates MAPK kinases (MAPKKs or MKKs or MAP2Ks) which in turn phosphorylate and activate MAPKs during signaling cascades that are important in mediating cellular responses to extracellular signals. MEKK4 activates the c-Jun N-terminal kinase (JNK) and p38 MAPK signaling pathways by directly activating their respective MAPKKs MKK4/MKK7 and MKK3/MKK6. JNK and p38 are collectively known as stress-activated MAPKs as they are activated in response to a variety of environmental stresses and pro-inflammatory cytokines. MEKK4 also plays roles in the re-polarization of the actin cytoskeleton in response to osmotic stress in the proper closure of the neural tube in cardiovascular development and in immune responses. |
gnl|CDD|132963 | 143 | 370 | 228 | Gaps:56 | 68.22 | 258 | 34.09 | 15.91 | 5e-09 | cd06632 STKc_MEKK1_plant Catalytic domain of the Protein Serine/Threonine Kinase Plant MAP/ERK kinase kinase 1. Serine/threonine kinases (STKs) plant MAP/ERK kinase kinase 1 (MEKK1)-like subfamily catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The plant MEKK1 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 is composed of plant mitogen-activated protein kinase (MAPK) kinase kinases (MAPKKKs or MKKKs or MAP3Ks) including Arabidopsis thaliana MEKK1 and MAPKKK3. MEKK1 is a MAPKKK that phosphorylates and activates MAPK kinases (MAPKKs or MKKs or MAP2Ks) which in turn phosphorylate and activate MAPKs during signaling cascades that are important in mediating cellular responses to extracellular signals. Arabidopsis thaliana MEKK1 activates MPK4 a MAPK that regulates systemic acquired resistance. MEKK1 also participates in the regulation of temperature-sensitive and tissue-specific cell death. |
gnl|CDD|173672 | 139 | 309 | 171 | Gaps:58 | 53.21 | 280 | 28.86 | 19.46 | 1e-08 | cd05581 STKc_PDK1 Catalytic domain of the Protein Serine/Threonine Kinase Phosphoinositide-dependent kinase 1. Serine/Threonine Kinases (STKs) Phosphoinositide-dependent kinase 1 (PDK1) subfamily catalytic (c) domain. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. The PDK1 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). PDK1 carries an N-terminal catalytic domain and a C-terminal pleckstrin homology (PH) domain that binds phosphoinositides. It phosphorylates the activation loop of AGC kinases that are regulated by PI3K such as PKB SGK and PKC among others and is crucial for their activation. Thus it contributes in regulating many processes including metabolism growth proliferation and survival. PDK1 also has the ability to autophosphorylate and is constitutively active in mammalian cells. PDK1 is essential for normal embryo development and is important in regulating cell volume. |
rpsblast_kog | gnl|CDD|35419 | 28 | 392 | 365 | Gaps:85 | 89.46 | 313 | 27.14 | 16.43 | 2e-14 | KOG0198 KOG0198 KOG0198 MEKK and related serine/threonine protein kinases [Signal transduction mechanisms]. |
gnl|CDD|35815 | 18 | 364 | 347 | Gaps:93 | 60.61 | 429 | 29.23 | 17.31 | 2e-10 | KOG0595 KOG0595 KOG0595 Serine/threonine-protein kinase involved in autophagy [Posttranslational modification protein turnover chaperones Intracellular trafficking secretion and vesicular transport Signal transduction mechanisms]. |
gnl|CDD|35835 | 133 | 369 | 237 | Gaps:51 | 41.26 | 475 | 32.65 | 18.37 | 1e-09 | KOG0615 KOG0615 KOG0615 Serine/threonine protein kinase Chk2 and related proteins [Cell cycle control cell division chromosome partitioning]. |
gnl|CDD|35818 | 109 | 374 | 266 | Gaps:67 | 62.46 | 357 | 27.35 | 17.04 | 3e-09 | KOG0598 KOG0598 KOG0598 Ribosomal protein S6 kinase and related proteins [General function prediction only Signal transduction mechanisms]. |
gnl|CDD|39451 | 29 | 309 | 281 | Gaps:80 | 28.55 | 732 | 30.14 | 16.75 | 5e-09 | KOG4250 KOG4250 KOG4250 TANK binding protein kinase TBK1 [Signal transduction mechanisms]. |
gnl|CDD|36366 | 209 | 368 | 160 | Gaps:12 | 19.10 | 775 | 33.78 | 17.57 | 7e-09 | KOG1151 KOG1151 KOG1151 Tousled-like protein kinase [Signal transduction mechanisms]. |
gnl|CDD|35805 | 143 | 368 | 226 | Gaps:43 | 31.77 | 576 | 29.51 | 20.77 | 9e-09 | KOG0585 KOG0585 KOG0585 Ca2+/calmodulin-dependent protein kinase kinase beta and related serine/threonine protein kinases [Signal transduction mechanisms]. |
gnl|CDD|35803 | 29 | 371 | 343 | Gaps:94 | 69.46 | 370 | 26.85 | 20.23 | 2e-08 | KOG0583 KOG0583 KOG0583 Serine/threonine protein kinase [Signal transduction mechanisms]. |
gnl|CDD|35255 | 199 | 369 | 171 | Gaps:25 | 38.22 | 382 | 28.77 | 15.07 | 8e-08 | KOG0032 KOG0032 KOG0032 Ca2+/calmodulin-dependent protein kinase EF-Hand protein superfamily [Signal transduction mechanisms]. |
gnl|CDD|37556 | 130 | 373 | 244 | Gaps:41 | 71.19 | 302 | 27.91 | 19.53 | 9e-08 | KOG2345 KOG2345 KOG2345 Serine/threonine protein kinase/TGF-beta stimulated factor [Transcription Lipid transport and metabolism Signal transduction mechanisms]. |