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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 2 |
GO:0005741 | mitochondrial outer membrane | 5 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0019867 | outer membrane | 3 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031966 | mitochondrial membrane | 4 | 2 |
GO:0031968 | organelle outer membrane | 4 | 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:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q906
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 477 | 481 | PF00656 | 0.502 |
CLV_MEL_PAP_1 | 259 | 265 | PF00089 | 0.548 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.523 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.782 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 376 | 378 | PF00082 | 0.672 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 506 | 508 | PF00082 | 0.782 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.715 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.481 |
DEG_APCC_DBOX_1 | 395 | 403 | PF00400 | 0.277 |
DEG_Kelch_actinfilin_1 | 528 | 532 | PF01344 | 0.234 |
DEG_SPOP_SBC_1 | 492 | 496 | PF00917 | 0.468 |
DOC_CKS1_1 | 32 | 37 | PF01111 | 0.491 |
DOC_MAPK_DCC_7 | 249 | 259 | PF00069 | 0.310 |
DOC_MAPK_gen_1 | 159 | 166 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 339 | 348 | PF00069 | 0.299 |
DOC_MAPK_JIP1_4 | 160 | 166 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 251 | 259 | PF00069 | 0.309 |
DOC_MAPK_RevD_3 | 532 | 548 | PF00069 | 0.371 |
DOC_PP2B_LxvP_1 | 277 | 280 | PF13499 | 0.330 |
DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.551 |
DOC_PP2B_PxIxI_1 | 254 | 260 | PF00149 | 0.315 |
DOC_PP4_FxxP_1 | 242 | 245 | PF00568 | 0.290 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 207 | 211 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.319 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 159 | 165 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 485 | 493 | PF00244 | 0.518 |
LIG_Actin_WH2_2 | 363 | 378 | PF00022 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 73 | 78 | PF00928 | 0.414 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.517 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.296 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.353 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.404 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.265 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.505 |
LIG_GBD_Chelix_1 | 366 | 374 | PF00786 | 0.573 |
LIG_LIR_Apic_2 | 240 | 245 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 404 | 413 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 451 | 460 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 522 | 532 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 522 | 527 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.364 |
LIG_Pex14_1 | 74 | 78 | PF04695 | 0.366 |
LIG_Pex14_2 | 301 | 305 | PF04695 | 0.272 |
LIG_Pex14_2 | 406 | 410 | PF04695 | 0.272 |
LIG_Rb_pABgroove_1 | 397 | 405 | PF01858 | 0.274 |
LIG_SH2_CRK | 329 | 333 | PF00017 | 0.288 |
LIG_SH2_GRB2like | 147 | 150 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 329 | 333 | PF00017 | 0.288 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.449 |
LIG_SH2_SRC | 53 | 56 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 147 | 151 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 362 | 366 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 403 | 407 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.457 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.495 |
LIG_SUMO_SIM_anti_2 | 540 | 545 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 444 | 451 | PF11976 | 0.420 |
LIG_TYR_ITIM | 331 | 336 | PF00017 | 0.308 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.487 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.474 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.315 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.499 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.502 |
MOD_CK2_1 | 353 | 359 | PF00069 | 0.418 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.418 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.733 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.743 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.708 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.716 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.713 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.662 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.493 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.658 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.533 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.718 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.620 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.705 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.702 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.208 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.522 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.592 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.507 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.513 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.374 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.368 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.470 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.525 |
MOD_LATS_1 | 209 | 215 | PF00433 | 0.524 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.471 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.577 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.331 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.432 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.401 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.500 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.383 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.327 |
MOD_NEK2_2 | 501 | 506 | PF00069 | 0.398 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.479 |
MOD_PIKK_1 | 485 | 491 | PF00454 | 0.446 |
MOD_PKA_1 | 211 | 217 | PF00069 | 0.430 |
MOD_PKA_1 | 506 | 512 | PF00069 | 0.577 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.579 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.548 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.422 |
MOD_Plk_2-3 | 385 | 391 | PF00069 | 0.345 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.325 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.335 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.469 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.513 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.313 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.528 |
MOD_SUMO_rev_2 | 73 | 81 | PF00179 | 0.389 |
TRG_DiLeu_BaEn_1 | 77 | 82 | PF01217 | 0.443 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 403 | 406 | PF00928 | 0.322 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.312 |
TRG_ER_diLys_1 | 547 | 550 | PF00400 | 0.693 |
TRG_NES_CRM1_1 | 297 | 310 | PF08389 | 0.363 |
TRG_NES_CRM1_1 | 379 | 391 | PF08389 | 0.363 |
TRG_NES_CRM1_1 | 455 | 466 | PF08389 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.680 |
TRG_Pf-PMV_PEXEL_1 | 462 | 466 | PF00026 | 0.718 |
TRG_Pf-PMV_PEXEL_1 | 79 | 83 | PF00026 | 0.602 |
TRG_Pf-PMV_PEXEL_1 | 91 | 96 | PF00026 | 0.600 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZG5 | Leptomonas seymouri | 64% | 96% |
A0A0S4IT25 | Bodo saltans | 45% | 80% |
A0A1X0P7G8 | Trypanosomatidae | 43% | 89% |
A0A3Q8IDW3 | Leishmania donovani | 96% | 100% |
A0A422NQN2 | Trypanosoma rangeli | 43% | 91% |
A4HF31 | Leishmania braziliensis | 88% | 100% |
A4I274 | Leishmania infantum | 96% | 100% |
C9ZX99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 91% |
E9AYG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |