blastp_kegg |
lcl|pmum:103322036
|
1 |
1377 |
+ |
1377 |
Gaps:9 |
100.00 |
1380 |
91.67 |
0.0 |
magnesium-chelatase subunit ChlH chloroplastic
|
blastp_kegg |
lcl|vvi:100258964
|
1 |
1377 |
+ |
1377 |
Gaps:8 |
100.00 |
1381 |
91.46 |
0.0 |
CHLH magnesium chelatase H subunit
|
blastp_kegg |
lcl|gmx:100806079
|
1 |
1377 |
+ |
1377 |
Gaps:7 |
100.00 |
1384 |
91.04 |
0.0 |
magnesium-chelatase subunit ChlH chloroplastic-like
|
blastp_kegg |
lcl|cmo:103499529
|
1 |
1377 |
+ |
1377 |
Gaps:7 |
100.00 |
1382 |
90.52 |
0.0 |
magnesium-chelatase subunit ChlH chloroplastic
|
blastp_kegg |
lcl|pvu:PHAVU_007G252700g
|
1 |
1377 |
+ |
1377 |
Gaps:10 |
100.00 |
1385 |
90.61 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|tcc:TCM_024638
|
1 |
1377 |
+ |
1377 |
Gaps:7 |
100.00 |
1382 |
90.96 |
0.0 |
Magnesium-chelatase subunit chl isoform 1
|
blastp_kegg |
lcl|gmx:548043
|
1 |
1377 |
+ |
1377 |
Gaps:8 |
100.00 |
1383 |
90.67 |
0.0 |
CHLH magnesium chelatase subunit
|
blastp_kegg |
lcl|gmx:100787735
|
1 |
1377 |
+ |
1377 |
Gaps:8 |
100.00 |
1383 |
90.74 |
0.0 |
magnesium-chelatase subunit ChlH chloroplastic-like
|
blastp_kegg |
lcl|csv:101213619
|
1 |
1377 |
+ |
1377 |
Gaps:7 |
100.00 |
1382 |
90.09 |
0.0 |
magnesium-chelatase subunit ChlH chloroplastic-like
|
blastp_kegg |
lcl|pxb:103933269
|
1 |
1377 |
+ |
1377 |
Gaps:9 |
100.00 |
1380 |
90.87 |
0.0 |
magnesium-chelatase subunit ChlH chloroplastic
|
blastp_uniprot_sprot |
sp|Q9FNB0|CHLH_ARATH
|
1 |
1377 |
+ |
1377 |
Gaps:14 |
100.00 |
1381 |
86.24 |
0.0 |
Magnesium-chelatase subunit ChlH chloroplastic OS Arabidopsis thaliana GN CHLH PE 1 SV 1
|
blastp_uniprot_sprot |
sp|B8ANF1|CHLH_ORYSI
|
1 |
1377 |
+ |
1377 |
Gaps:14 |
100.00 |
1387 |
84.07 |
0.0 |
Magnesium-chelatase subunit ChlH chloroplastic OS Oryza sativa subsp. indica GN CHLH PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q10M50|CHLH_ORYSJ
|
1 |
1377 |
+ |
1377 |
Gaps:14 |
100.00 |
1387 |
83.92 |
0.0 |
Magnesium-chelatase subunit ChlH chloroplastic OS Oryza sativa subsp. japonica GN CHLH PE 1 SV 1
|
blastp_uniprot_sprot |
sp|O50314|BCHH_CHLP8
|
153 |
1375 |
+ |
1223 |
Gaps:106 |
94.73 |
1272 |
34.61 |
0.0 |
Magnesium-chelatase subunit H OS Chlorobaculum parvum (strain NCIB 8327) GN bchH PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q9RFD5|BCHH_RHOS4
|
77 |
1375 |
+ |
1299 |
Gaps:77 |
97.15 |
1193 |
41.16 |
5e-160 |
Magnesium-chelatase subunit H OS Rhodobacter sphaeroides (strain ATCC 17023 / 2.4.1 / NCIB 8253 / DSM 158) GN bchH PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P26162|BCHH_RHOCB
|
139 |
1375 |
+ |
1237 |
Gaps:76 |
93.19 |
1189 |
41.43 |
1e-155 |
Magnesium-chelatase subunit H OS Rhodobacter capsulatus (strain ATCC BAA-309 / NBRC 16581 / SB1003) GN bchH PE 3 SV 2
|
blastp_uniprot_sprot |
sp|Q58318|Y908_METJA
|
255 |
1373 |
+ |
1119 |
Gaps:103 |
89.61 |
1232 |
31.88 |
2e-155 |
Uncharacterized protein MJ0908 OS Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN MJ0908 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q58836|Y1441_METJA
|
326 |
1373 |
+ |
1048 |
Gaps:138 |
84.99 |
1226 |
32.53 |
2e-133 |
Uncharacterized protein MJ1441 OS Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN MJ1441 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q9HZQ3|COBN_PSEAE
|
324 |
1371 |
+ |
1048 |
Gaps:105 |
84.05 |
1248 |
30.60 |
8e-127 |
Aerobic cobaltochelatase subunit CobN OS Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN cobN PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P29929|COBN_PSEDE
|
285 |
1361 |
+ |
1077 |
Gaps:107 |
85.18 |
1275 |
30.20 |
3e-121 |
Aerobic cobaltochelatase subunit CobN OS Pseudomonas denitrificans GN cobN PE 1 SV 1
|
rpsblast_cdd |
gnl|CDD|178618
|
59 |
1256 |
+ |
1198 |
Gaps:7 |
98.77 |
1220 |
84.98 |
0.0 |
PLN03069 PLN03069 magnesiumprotoporphyrin-IX chelatase subunit H Provisional.
|
rpsblast_cdd |
gnl|CDD|183556
|
67 |
1376 |
+ |
1310 |
Gaps:25 |
99.77 |
1310 |
63.05 |
0.0 |
PRK12493 PRK12493 magnesium chelatase subunit H Provisional.
|
rpsblast_cdd |
gnl|CDD|188195
|
82 |
1375 |
+ |
1294 |
Gaps:97 |
99.92 |
1224 |
50.61 |
0.0 |
TIGR02025 BchH magnesium chelatase H subunit. This model represents the H subunit of the magnesium chelatase complex responsible for magnesium insertion into the protoporphyrin IX ring in the biosynthesis of both chlorophyll and bacteriochlorophyll. In chlorophyll-utilizing species this gene is known as ChlH while in bacteriochlorophyll-utilizing spoecies it is called BchH. Subunit H is the largest (~140kDa) of the three subunits (the others being BchD/ChlD and BchI/ChlI) and is known to bind protoporphyrin IX. Subunit H is homologous to the CobN subunit of cobaltochelatase and by anology with that enzyme subunit H is believed to also bind the magnesium ion which is inserted into the ring. In conjunction with the hydrolysis of ATP by subunits I and D a conformation change is believed to happen in subunit H causing the magnesium ion insertion into the distorted protoporphyrin ring.
|
rpsblast_cdd |
gnl|CDD|202267
|
245 |
1359 |
+ |
1115 |
Gaps:123 |
99.91 |
1079 |
42.12 |
0.0 |
pfam02514 CobN-Mg_chel CobN/Magnesium Chelatase. This family contains a domain common to the cobN protein and to magnesium protoporphyrin chelatase. CobN is implicated in the conversion of hydrogenobyrinic acid a c-diamide to cobyrinic acid. Magnesium protoporphyrin chelatase is involved in chlorophyll biosynthesis.
|
rpsblast_cdd |
gnl|CDD|31618
|
229 |
1374 |
+ |
1146 |
Gaps:85 |
81.92 |
1388 |
38.52 |
0.0 |
COG1429 CobN Cobalamin biosynthesis protein CobN and related Mg-chelatases [Coenzyme metabolism].
|
rpsblast_cdd |
gnl|CDD|180340
|
214 |
1369 |
+ |
1156 |
Gaps:121 |
92.04 |
1244 |
32.75 |
0.0 |
PRK05989 cobN cobaltochelatase subunit CobN Reviewed.
|
rpsblast_cdd |
gnl|CDD|184034
|
79 |
1375 |
+ |
1297 |
Gaps:89 |
97.93 |
1209 |
42.57 |
0.0 |
PRK13405 bchH magnesium chelatase subunit H Provisional.
|
rpsblast_cdd |
gnl|CDD|199903
|
157 |
1248 |
+ |
1092 |
Gaps:140 |
100.00 |
910 |
41.21 |
1e-168 |
cd10150 CobN_like CobN subunit of cobaltochelatase bchH and chlH subunits of magnesium chelatases and similar proteins. Cobaltochelatase is a complex enzyme that catalyzes the insertion of cobalt into hydrogenobyrinic acid a c-diamide resulting in cobyrinic acid as demonstrated for Pseudomonas denitrificans. This is an essential step in the bacterial synthesis of cobalamine (B12). The insertion of cobalt requires a complex composed of three polypeptides cobN cobS and cobT. Also included in this family are protoporphyrin IX magnesium chelatases involved in the synthesis of chlorophyll and bacteriochlorophyll specifically the large (chlH or bchH) subunits.They are thought to bind both the protoporphyrin and the magnesium ion. Hydrolysis of ATP by the smaller subunits in the complex may trigger a conformational change that results in the insertion of the ion into the protoporphyrin scaffold. Cryo electron microscopy studies have suggested that a distinct bchH C-terminal domain may bind tightly to the N-terminal domain upon substrate binding requiring a substantial conformational change of the bchH subunit. It has also been suggested that chlH of higher plants binds abscisic acid via a C-terminal domain and plays a role in abscisic acid signaling and that the protein spans the chloroplast envelope with the C-terminus exposed to the cytosol.
|
rpsblast_cdd |
gnl|CDD|178779
|
123 |
1375 |
+ |
1253 |
Gaps:118 |
83.67 |
1353 |
35.16 |
1e-107 |
PLN03241 PLN03241 magnesium chelatase subunit H Provisional.
|
rpsblast_cdd |
gnl|CDD|131310
|
214 |
1369 |
+ |
1156 |
Gaps:119 |
91.27 |
1122 |
31.35 |
2e-76 |
TIGR02257 cobalto_cobN cobaltochelatase CobN subunit.
|