Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HIE1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004022 | alcohol dehydrogenase (NAD+) activity | 6 | 6 |
GO:0005488 | binding | 1 | 8 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 8 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 8 |
GO:0018455 | alcohol dehydrogenase [NAD(P)+] activity | 5 | 6 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.384 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.476 |
DOC_CDC14_PxL_1 | 140 | 148 | PF14671 | 0.476 |
DOC_CDC14_PxL_1 | 31 | 39 | PF14671 | 0.476 |
DOC_CKS1_1 | 180 | 185 | PF01111 | 0.405 |
DOC_CKS1_1 | 19 | 24 | PF01111 | 0.367 |
DOC_CYCLIN_RxL_1 | 39 | 51 | PF00134 | 0.360 |
DOC_MAPK_gen_1 | 39 | 49 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 97 | 107 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 136 | 142 | PF00149 | 0.405 |
DOC_PP4_FxxP_1 | 180 | 183 | PF00568 | 0.476 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.473 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.377 |
LIG_14-3-3_CanoR_1 | 125 | 132 | PF00244 | 0.229 |
LIG_14-3-3_CanoR_1 | 357 | 361 | PF00244 | 0.229 |
LIG_AP2alpha_2 | 178 | 180 | PF02296 | 0.476 |
LIG_APCC_ABBA_1 | 74 | 79 | PF00400 | 0.405 |
LIG_EVH1_1 | 141 | 145 | PF00568 | 0.476 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.517 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.316 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.421 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.311 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.287 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.229 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.341 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.327 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.229 |
LIG_LIR_Apic_2 | 178 | 183 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 172 | 181 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 214 | 222 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 392 | 399 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 260 | 265 | PF02991 | 0.229 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.457 |
LIG_MYND_1 | 179 | 183 | PF01753 | 0.405 |
LIG_PCNA_PIPBox_1 | 233 | 242 | PF02747 | 0.405 |
LIG_Pex14_2 | 137 | 141 | PF04695 | 0.229 |
LIG_PTB_Apo_2 | 374 | 381 | PF02174 | 0.405 |
LIG_PTB_Phospho_1 | 374 | 380 | PF10480 | 0.405 |
LIG_SH2_CRK | 286 | 290 | PF00017 | 0.352 |
LIG_SH2_CRK | 380 | 384 | PF00017 | 0.476 |
LIG_SH2_GRB2like | 216 | 219 | PF00017 | 0.405 |
LIG_SH2_GRB2like | 292 | 295 | PF00017 | 0.476 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.238 |
LIG_SH2_SRC | 292 | 295 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.383 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.476 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.448 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.422 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.451 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.458 |
LIG_SUMO_SIM_par_1 | 145 | 152 | PF11976 | 0.352 |
LIG_SUMO_SIM_par_1 | 189 | 195 | PF11976 | 0.329 |
LIG_TYR_ITIM | 75 | 80 | PF00017 | 0.229 |
LIG_WRC_WIRS_1 | 60 | 65 | PF05994 | 0.229 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.352 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.322 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.367 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.406 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.229 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.396 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.305 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.352 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.444 |
MOD_N-GLC_2 | 99 | 101 | PF02516 | 0.352 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.485 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.381 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.476 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.389 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.348 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.392 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.291 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.229 |
MOD_NEK2_2 | 356 | 361 | PF00069 | 0.229 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.229 |
MOD_PKB_1 | 18 | 26 | PF00069 | 0.307 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.352 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.389 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.483 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.381 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.458 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.291 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.352 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.375 |
TRG_DiLeu_BaEn_1 | 340 | 345 | PF01217 | 0.229 |
TRG_DiLeu_BaEn_4 | 90 | 96 | PF01217 | 0.476 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMM0 | Leptomonas seymouri | 64% | 98% |
A0A0N1P9Y7 | Leptomonas seymouri | 36% | 100% |
A0A0S1X9S7 | Thermococcus barophilus | 31% | 100% |
A0A1X0P6U8 | Trypanosomatidae | 37% | 100% |
A0A3R7LCK2 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X3G7 | Leishmania donovani | 81% | 100% |
A4I5N8 | Leishmania infantum | 81% | 100% |
A4IP64 | Geobacillus thermodenitrificans (strain NG80-2) | 36% | 100% |
A4ISB9 | Geobacillus thermodenitrificans (strain NG80-2) | 27% | 100% |
A6QP15 | Bos taurus | 28% | 86% |
A6ZTT5 | Saccharomyces cerevisiae (strain YJM789) | 33% | 100% |
A8WTJ7 | Caenorhabditis briggsae | 30% | 86% |
B1VB76 | Citrobacter freundii | 31% | 100% |
C5MRT8 | Mycobacterium sp. (strain DSM 3803 / JC1) | 34% | 94% |
E5Y946 | Bilophila wadsworthia (strain 3_1_6) | 27% | 100% |
E9B0Y2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
F8DVL8 | Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) | 39% | 100% |
O05239 | Bacillus subtilis (strain 168) | 29% | 100% |
O05240 | Bacillus subtilis (strain 168) | 28% | 100% |
O30847 | Pseudomonas knackmussii (strain DSM 6978 / LMG 23759 / B13) | 25% | 100% |
O87612 | Pseudomonas aeruginosa | 25% | 100% |
P0A9S1 | Escherichia coli (strain K12) | 34% | 100% |
P0A9S2 | Escherichia coli O157:H7 | 34% | 100% |
P0DJA2 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 39% | 100% |
P10127 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
P13604 | Clostridium saccharobutylicum | 32% | 100% |
P27101 | Pseudomonas sp. (strain P51) | 25% | 100% |
P27137 | Cupriavidus pinatubonensis (strain JMP 134 / LMG 1197) | 24% | 100% |
P31005 | Bacillus methanolicus | 34% | 100% |
P37686 | Escherichia coli (strain K12) | 38% | 100% |
P41795 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 32% | 100% |
P45513 | Citrobacter freundii | 37% | 100% |
P71017 | Bacillus subtilis (strain 168) | 36% | 99% |
P76553 | Escherichia coli (strain K12) | 33% | 100% |
Q08B39 | Xenopus laevis | 28% | 86% |
Q09669 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 95% |
Q17EN4 | Aedes aegypti | 27% | 86% |
Q24857 | Entamoeba histolytica | 24% | 100% |
Q28XT3 | Drosophila pseudoobscura pseudoobscura | 30% | 86% |
Q45072 | Burkholderia cepacia | 25% | 100% |
Q46856 | Escherichia coli (strain K12) | 28% | 100% |
Q4Q784 | Leishmania major | 80% | 100% |
Q4QQW3 | Rattus norvegicus | 28% | 85% |
Q53062 | Rhodococcus erythropolis | 32% | 94% |
Q54GJ7 | Dictyostelium discoideum | 26% | 73% |
Q59104 | Cupriavidus necator | 35% | 100% |
Q59477 | Klebsiella pneumoniae | 37% | 100% |
Q5RF11 | Pongo abelii | 28% | 85% |
Q6P371 | Xenopus tropicalis | 29% | 86% |
Q7Q547 | Anopheles gambiae | 28% | 86% |
Q8IWW8 | Homo sapiens | 28% | 85% |
Q8R0N6 | Mus musculus | 29% | 86% |
Q93T12 | Delftia acidovorans | 25% | 100% |
Q9F282 | Thermoanaerobacter ethanolicus | 30% | 100% |
Q9RCG0 | Amycolatopsis methanolica | 32% | 93% |
Q9U2M4 | Caenorhabditis elegans | 32% | 86% |
Q9W265 | Drosophila melanogaster | 28% | 86% |
Q9XDN0 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 32% | 100% |
V5BRQ8 | Trypanosoma cruzi | 39% | 100% |