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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H649
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 17 |
GO:0016491 | oxidoreductase activity | 2 | 17 |
GO:0003960 | NADPH:quinone reductase activity | 5 | 1 |
GO:0016651 | oxidoreductase activity, acting on NAD(P)H | 3 | 1 |
GO:0016655 | oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.250 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.415 |
CLV_PCSK_FUR_1 | 437 | 441 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.497 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.335 |
DEG_APCC_DBOX_1 | 375 | 383 | PF00400 | 0.453 |
DOC_CKS1_1 | 346 | 351 | PF01111 | 0.283 |
DOC_MAPK_FxFP_2 | 122 | 125 | PF00069 | 0.437 |
DOC_MAPK_JIP1_4 | 30 | 36 | PF00069 | 0.538 |
DOC_PP1_RVXF_1 | 167 | 173 | PF00149 | 0.386 |
DOC_PP1_RVXF_1 | 215 | 222 | PF00149 | 0.455 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.437 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.527 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 112 | 120 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 356 | 362 | PF00244 | 0.326 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.554 |
LIG_APCC_ABBA_1 | 306 | 311 | PF00400 | 0.181 |
LIG_BRCT_BRCA1_1 | 203 | 207 | PF00533 | 0.381 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.401 |
LIG_eIF4E_1 | 313 | 319 | PF01652 | 0.401 |
LIG_EVH1_2 | 120 | 124 | PF00568 | 0.456 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.584 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.364 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.253 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.232 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.395 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.348 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.566 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.313 |
LIG_LIR_Apic_2 | 193 | 199 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 233 | 242 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 360 | 368 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 183 | 187 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.310 |
LIG_MYND_1 | 27 | 31 | PF01753 | 0.636 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.466 |
LIG_SH2_NCK_1 | 187 | 191 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 446 | 450 | PF00017 | 0.613 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.552 |
LIG_SH2_PTP2 | 235 | 238 | PF00017 | 0.342 |
LIG_SH2_PTP2 | 363 | 366 | PF00017 | 0.326 |
LIG_SH2_SRC | 273 | 276 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.504 |
LIG_SH3_1 | 19 | 25 | PF00018 | 0.561 |
LIG_SH3_2 | 118 | 123 | PF14604 | 0.481 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.562 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.605 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.607 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.717 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.681 |
LIG_SUMO_SIM_anti_2 | 408 | 416 | PF11976 | 0.423 |
LIG_TYR_ITIM | 361 | 366 | PF00017 | 0.345 |
LIG_WW_1 | 16 | 19 | PF00397 | 0.552 |
MOD_CDK_SPxxK_3 | 277 | 284 | PF00069 | 0.310 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.488 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.317 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.288 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.653 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.679 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.376 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.603 |
MOD_GlcNHglycan | 148 | 154 | PF01048 | 0.744 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.473 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.444 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.345 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.547 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.509 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.647 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.682 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.687 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.688 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.266 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.646 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.701 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.389 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.629 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.566 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.216 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.532 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.522 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.468 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.380 |
MOD_PK_1 | 357 | 363 | PF00069 | 0.345 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.640 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.283 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.471 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.428 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.398 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.393 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.552 |
TRG_DiLeu_BaEn_2 | 399 | 405 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 214 | 219 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.326 |
TRG_ER_diArg_1 | 355 | 357 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 437 | 440 | PF00400 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0C6DWS6 | Neocamarosporium betae | 24% | 100% |
A0A0N0P3I0 | Leptomonas seymouri | 24% | 100% |
A0A0N0P5I8 | Leptomonas seymouri | 45% | 100% |
A0A0N1I4X2 | Leptomonas seymouri | 69% | 100% |
A0A0S4ILS9 | Bodo saltans | 28% | 100% |
A0A0S4JMB1 | Bodo saltans | 27% | 100% |
A0A1X0NRR2 | Trypanosomatidae | 45% | 98% |
A0A3Q8IRG0 | Leishmania donovani | 27% | 100% |
A0A3S7WR50 | Leishmania donovani | 43% | 100% |
A0A3S7WR58 | Leishmania donovani | 85% | 100% |
A0A3S7X2E3 | Leishmania donovani | 26% | 100% |
A4H648 | Leishmania braziliensis | 43% | 98% |
A4HUG8 | Leishmania infantum | 43% | 100% |
A4HUG9 | Leishmania infantum | 85% | 100% |
A4I4G0 | Leishmania infantum | 26% | 100% |
A4IE56 | Leishmania infantum | 27% | 100% |
C9ZVI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AN66 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9ATK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 91% |
K4BW79 | Solanum lycopersicum | 29% | 100% |
O94038 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 28% | 100% |
O94564 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 100% |
Q0CJC5 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 27% | 100% |
Q0VC50 | Bos taurus | 25% | 100% |
Q24K16 | Bos taurus | 25% | 100% |
Q4QHF8 | Leishmania major | 84% | 100% |
Q4QHF9 | Leishmania major | 44% | 97% |
Q4W4Z2 | Caenorhabditis elegans | 27% | 100% |
Q5HM44 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 25% | 100% |
Q5JI69 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 24% | 100% |
Q7T3C7 | Danio rerio | 25% | 100% |
Q84V25 | Fragaria ananassa | 25% | 100% |
Q8BGC4 | Mus musculus | 22% | 100% |
Q8CRJ7 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 25% | 100% |
Q8H0M1 | Spinacia oleracea | 26% | 100% |
Q8JFV8 | Danio rerio | 25% | 99% |
Q8KQL2 | Enterococcus avium | 21% | 100% |
Q8N4Q0 | Homo sapiens | 25% | 100% |
Q8WWV3 | Homo sapiens | 25% | 100% |
Q924D0 | Mus musculus | 25% | 100% |
Q99536 | Homo sapiens | 26% | 100% |
Q9AYU1 | Triphysaria versicolor | 24% | 100% |
Q9SV68 | Arabidopsis thaliana | 25% | 100% |
Q9ZUC1 | Arabidopsis thaliana | 28% | 100% |
V5ALK9 | Trypanosoma cruzi | 47% | 100% |
V5B1P3 | Trypanosoma cruzi | 29% | 100% |