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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 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: A0A3Q8IAB6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 449 | 453 | PF00656 | 0.481 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 14 | 16 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 410 | 412 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.480 |
CLV_PCSK_PC7_1 | 532 | 538 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 481 | 485 | PF00082 | 0.773 |
CLV_Separin_Metazoa | 528 | 532 | PF03568 | 0.544 |
DEG_APCC_DBOX_1 | 154 | 162 | PF00400 | 0.492 |
DEG_APCC_DBOX_1 | 345 | 353 | PF00400 | 0.402 |
DEG_SPOP_SBC_1 | 27 | 31 | PF00917 | 0.492 |
DOC_CYCLIN_RxL_1 | 350 | 359 | PF00134 | 0.416 |
DOC_CYCLIN_yClb1_LxF_4 | 220 | 226 | PF00134 | 0.382 |
DOC_MAPK_FxFP_2 | 366 | 369 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 102 | 110 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 14 | 20 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 398 | 406 | PF00069 | 0.605 |
DOC_PP2B_LxvP_1 | 355 | 358 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.606 |
DOC_PP4_FxxP_1 | 366 | 369 | PF00568 | 0.569 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.493 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.558 |
DOC_USP7_MATH_2 | 57 | 63 | PF00917 | 0.532 |
DOC_USP7_UBL2_3 | 328 | 332 | PF12436 | 0.614 |
DOC_USP7_UBL2_3 | 468 | 472 | PF12436 | 0.666 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 26 | 32 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 340 | 348 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 35 | 41 | PF00244 | 0.688 |
LIG_Actin_WH2_2 | 401 | 416 | PF00022 | 0.639 |
LIG_Clathr_ClatBox_1 | 162 | 166 | PF01394 | 0.387 |
LIG_deltaCOP1_diTrp_1 | 117 | 122 | PF00928 | 0.603 |
LIG_deltaCOP1_diTrp_1 | 400 | 406 | PF00928 | 0.553 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.727 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.336 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.706 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.455 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.327 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.549 |
LIG_GBD_Chelix_1 | 384 | 392 | PF00786 | 0.416 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 156 | 165 | PF02991 | 0.270 |
LIG_LIR_Gen_1 | 218 | 226 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 400 | 408 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 218 | 222 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.504 |
LIG_NRBOX | 351 | 357 | PF00104 | 0.514 |
LIG_PCNA_yPIPBox_3 | 90 | 103 | PF02747 | 0.459 |
LIG_Pex14_2 | 207 | 211 | PF04695 | 0.560 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.515 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.523 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.243 |
LIG_SH2_CRK | 219 | 223 | PF00017 | 0.407 |
LIG_SH2_GRB2like | 219 | 222 | PF00017 | 0.412 |
LIG_SH2_GRB2like | 276 | 279 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 159 | 163 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 219 | 223 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.547 |
LIG_SH2_STAT3 | 444 | 447 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.402 |
LIG_SH3_1 | 252 | 258 | PF00018 | 0.403 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.463 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.610 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.727 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.577 |
LIG_SUMO_SIM_par_1 | 371 | 377 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 383 | 389 | PF11976 | 0.451 |
LIG_TRAF2_1 | 333 | 336 | PF00917 | 0.616 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.519 |
LIG_TYR_ITIM | 110 | 115 | PF00017 | 0.577 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.626 |
MOD_CDC14_SPxK_1 | 11 | 14 | PF00782 | 0.473 |
MOD_CDK_SPxK_1 | 8 | 14 | PF00069 | 0.509 |
MOD_CDK_SPxxK_3 | 8 | 15 | PF00069 | 0.493 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.564 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.552 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.526 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.438 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.782 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.487 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.773 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.642 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.637 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.553 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.602 |
MOD_Cter_Amidation | 100 | 103 | PF01082 | 0.462 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.528 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.742 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.746 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.701 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.568 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.590 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.498 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.609 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.703 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.786 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.592 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.530 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.697 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.663 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.703 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.481 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.686 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.755 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.572 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.506 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.458 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.616 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.545 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.675 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.558 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.437 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.677 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.425 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.609 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.553 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.694 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.552 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.474 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.341 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.542 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.634 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.491 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.600 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.509 |
MOD_SUMO_for_1 | 163 | 166 | PF00179 | 0.436 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.660 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.608 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.680 |
TRG_ER_diArg_1 | 530 | 532 | PF00400 | 0.554 |
TRG_NES_CRM1_1 | 347 | 361 | PF08389 | 0.413 |
TRG_NLS_MonoExtC_3 | 460 | 465 | PF00514 | 0.535 |
TRG_NLS_MonoExtN_4 | 410 | 415 | PF00514 | 0.726 |
TRG_Pf-PMV_PEXEL_1 | 346 | 351 | PF00026 | 0.333 |
TRG_Pf-PMV_PEXEL_1 | 411 | 415 | PF00026 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 438 | 442 | PF00026 | 0.672 |
TRG_Pf-PMV_PEXEL_1 | 95 | 100 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P950 | Leptomonas seymouri | 23% | 97% |
A0A0N1ILX4 | Leptomonas seymouri | 60% | 100% |
A0A0S4JKE9 | Bodo saltans | 50% | 100% |
A0A1X0NTZ8 | Trypanosomatidae | 55% | 100% |
A0A3S5IRP3 | Trypanosoma rangeli | 53% | 100% |
A0A3S7X2J5 | Leishmania donovani | 26% | 100% |
A4H889 | Leishmania braziliensis | 84% | 99% |
A4HHF5 | Leishmania braziliensis | 25% | 100% |
A4HWL2 | Leishmania infantum | 99% | 100% |
A4I4K3 | Leishmania infantum | 25% | 100% |
C9ZL87 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZXS8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AE02 | Leishmania major | 25% | 100% |
E9ALT0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AQB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4QF55 | Leishmania major | 95% | 100% |
V5B4N1 | Trypanosoma cruzi | 55% | 100% |
V5D9T1 | Trypanosoma cruzi | 24% | 100% |