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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005747 | mitochondrial respiratory chain complex I | 4 | 1 |
GO:0030964 | NADH dehydrogenase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0045271 | respiratory chain complex I | 4 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 1 |
GO:0098803 | respiratory chain complex | 3 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902495 | transmembrane transporter complex | 3 | 1 |
GO:1990204 | oxidoreductase complex | 3 | 1 |
GO:1990351 | transporter complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7WVT1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.393 |
CLV_C14_Caspase3-7 | 546 | 550 | PF00656 | 0.415 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.421 |
CLV_PCSK_FUR_1 | 235 | 239 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.629 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.481 |
DEG_Kelch_Keap1_1 | 15 | 20 | PF01344 | 0.652 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.696 |
DEG_ODPH_VHL_1 | 475 | 488 | PF01847 | 0.375 |
DEG_SPOP_SBC_1 | 164 | 168 | PF00917 | 0.570 |
DOC_CDC14_PxL_1 | 203 | 211 | PF14671 | 0.407 |
DOC_CDC14_PxL_1 | 41 | 49 | PF14671 | 0.503 |
DOC_CYCLIN_RxL_1 | 432 | 443 | PF00134 | 0.358 |
DOC_CYCLIN_yCln2_LP_2 | 326 | 332 | PF00134 | 0.457 |
DOC_MAPK_gen_1 | 123 | 133 | PF00069 | 0.399 |
DOC_MAPK_gen_1 | 234 | 244 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 452 | 460 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 125 | 134 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 184 | 192 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 499 | 507 | PF00069 | 0.524 |
DOC_PP1_RVXF_1 | 434 | 441 | PF00149 | 0.349 |
DOC_PP2B_LxvP_1 | 535 | 538 | PF13499 | 0.528 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.533 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 229 | 236 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 32 | 40 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 389 | 394 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 499 | 504 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 98 | 105 | PF00244 | 0.365 |
LIG_BRCT_BRCA1_1 | 389 | 393 | PF00533 | 0.393 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.397 |
LIG_Clathr_ClatBox_1 | 131 | 135 | PF01394 | 0.349 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.419 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.414 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.698 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.308 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.341 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.347 |
LIG_FHA_2 | 260 | 266 | PF00498 | 0.501 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.461 |
LIG_LIR_Gen_1 | 152 | 162 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 518 | 524 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 60 | 66 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.367 |
LIG_LIR_LC3C_4 | 129 | 134 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 518 | 523 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.372 |
LIG_NRP_CendR_1 | 553 | 556 | PF00754 | 0.611 |
LIG_Pex14_1 | 409 | 413 | PF04695 | 0.414 |
LIG_Pex14_1 | 516 | 520 | PF04695 | 0.456 |
LIG_Pex14_2 | 307 | 311 | PF04695 | 0.489 |
LIG_PTB_Apo_2 | 199 | 206 | PF02174 | 0.456 |
LIG_PTB_Phospho_1 | 199 | 205 | PF10480 | 0.458 |
LIG_SH2_CRK | 42 | 46 | PF00017 | 0.518 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.419 |
LIG_SH2_NCK_1 | 366 | 370 | PF00017 | 0.344 |
LIG_SH2_PTP2 | 205 | 208 | PF00017 | 0.378 |
LIG_SH2_SRC | 478 | 481 | PF00017 | 0.383 |
LIG_SH2_STAP1 | 413 | 417 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.383 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.402 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.407 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.342 |
LIG_SUMO_SIM_anti_2 | 129 | 136 | PF11976 | 0.357 |
LIG_SUMO_SIM_anti_2 | 141 | 149 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 484 | 491 | PF11976 | 0.486 |
LIG_SUMO_SIM_anti_2 | 502 | 507 | PF11976 | 0.519 |
LIG_SUMO_SIM_par_1 | 129 | 136 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 239 | 245 | PF11976 | 0.389 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.396 |
LIG_TRAF2_1 | 418 | 421 | PF00917 | 0.563 |
LIG_TRAF2_1 | 508 | 511 | PF00917 | 0.533 |
LIG_TYR_ITIM | 203 | 208 | PF00017 | 0.400 |
LIG_UBA3_1 | 437 | 442 | PF00899 | 0.491 |
LIG_UBA3_1 | 519 | 526 | PF00899 | 0.407 |
MOD_CDK_SPK_2 | 305 | 310 | PF00069 | 0.448 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.611 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.537 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.688 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.425 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.504 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.517 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.435 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.631 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.650 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.484 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.490 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.657 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.458 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.490 |
MOD_GlcNHglycan | 388 | 392 | PF01048 | 0.370 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.405 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.501 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.542 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.419 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.674 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.354 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.503 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.406 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.399 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.547 |
MOD_N-GLC_1 | 484 | 489 | PF02516 | 0.443 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.434 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.364 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.405 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.309 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.365 |
MOD_NEK2_1 | 515 | 520 | PF00069 | 0.295 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.498 |
MOD_NEK2_2 | 295 | 300 | PF00069 | 0.533 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.512 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.541 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.439 |
MOD_PK_1 | 499 | 505 | PF00069 | 0.485 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.648 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.448 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.392 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.525 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.526 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.561 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.491 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.493 |
MOD_Plk_2-3 | 31 | 37 | PF00069 | 0.648 |
MOD_Plk_2-3 | 484 | 490 | PF00069 | 0.391 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.439 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.441 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.453 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.467 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.401 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.341 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.521 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.374 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.505 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.467 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.547 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.465 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.463 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.481 |
MOD_SUMO_for_1 | 309 | 312 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 546 | 555 | PF00179 | 0.469 |
TRG_DiLeu_BaEn_1 | 127 | 132 | PF01217 | 0.376 |
TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_1 | 433 | 438 | PF01217 | 0.354 |
TRG_DiLeu_BaEn_4 | 510 | 516 | PF01217 | 0.329 |
TRG_DiLeu_BaLyEn_6 | 204 | 209 | PF01217 | 0.352 |
TRG_DiLeu_LyEn_5 | 36 | 41 | PF01217 | 0.619 |
TRG_DiLeu_LyEn_5 | 433 | 438 | PF01217 | 0.354 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 71 | 74 | PF00928 | 0.417 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 350 | 353 | PF00400 | 0.441 |
TRG_ER_diLys_1 | 553 | 556 | PF00400 | 0.546 |
TRG_NES_CRM1_1 | 484 | 497 | PF08389 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 184 | 189 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 429 | 433 | PF00026 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 513 | 517 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 59 | 63 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P560 | Leptomonas seymouri | 71% | 100% |
A0A0S4JGE1 | Bodo saltans | 34% | 94% |
A0A1X0NY36 | Trypanosomatidae | 44% | 98% |
A0A422N7U6 | Trypanosoma rangeli | 38% | 100% |
A4HBI0 | Leishmania braziliensis | 86% | 100% |
A4HYK2 | Leishmania infantum | 100% | 100% |
C9ZHV1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 98% |
E9AUF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4QD32 | Leishmania major | 94% | 100% |
V5BAF5 | Trypanosoma cruzi | 45% | 99% |