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:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9ADR7
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 8 |
GO:0006811 | monoatomic ion transport | 4 | 8 |
GO:0006817 | phosphate ion transport | 7 | 8 |
GO:0006820 | monoatomic anion transport | 5 | 8 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015698 | inorganic anion transport | 6 | 8 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0035435 | phosphate ion transmembrane transport | 6 | 2 |
GO:0051179 | localization | 1 | 8 |
GO:0051234 | establishment of localization | 2 | 8 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 2 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 2 |
GO:0098661 | inorganic anion transmembrane transport | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 8 |
GO:0005315 | inorganic phosphate transmembrane transporter activity | 4 | 8 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 8 |
GO:0015293 | symporter activity | 5 | 8 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 8 |
GO:0022804 | active transmembrane transporter activity | 3 | 8 |
GO:0022857 | transmembrane transporter activity | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.500 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 358 | 360 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.226 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.193 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 680 | 684 | PF00082 | 0.258 |
DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.323 |
DOC_CYCLIN_yCln2_LP_2 | 533 | 539 | PF00134 | 0.466 |
DOC_MAPK_DCC_7 | 79 | 88 | PF00069 | 0.277 |
DOC_MAPK_gen_1 | 409 | 416 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 492 | 500 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 145 | 154 | PF00069 | 0.238 |
DOC_MAPK_MEF2A_6 | 92 | 99 | PF00069 | 0.241 |
DOC_PP1_RVXF_1 | 284 | 291 | PF00149 | 0.464 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.323 |
DOC_PP2B_LxvP_1 | 336 | 339 | PF13499 | 0.500 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.435 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.285 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.500 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 422 | 427 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 500 | 505 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 182 | 187 | PF00244 | 0.416 |
LIG_APCC_ABBA_1 | 428 | 433 | PF00400 | 0.393 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.270 |
LIG_BRCT_BRCA1_1 | 37 | 41 | PF00533 | 0.435 |
LIG_CaM_NSCaTE_8 | 630 | 637 | PF13499 | 0.311 |
LIG_CtBP_PxDLS_1 | 649 | 653 | PF00389 | 0.235 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.235 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.329 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.270 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.275 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.482 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.498 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.490 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.333 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.270 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.278 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.292 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.285 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.270 |
LIG_GBD_Chelix_1 | 686 | 694 | PF00786 | 0.302 |
LIG_Integrin_RGD_1 | 294 | 296 | PF01839 | 0.264 |
LIG_IRF3_LxIS_1 | 686 | 692 | PF10401 | 0.269 |
LIG_LIR_Apic_2 | 113 | 119 | PF02991 | 0.435 |
LIG_LIR_Apic_2 | 142 | 146 | PF02991 | 0.249 |
LIG_LIR_Apic_2 | 372 | 378 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 204 | 215 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 38 | 45 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 569 | 579 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 590 | 600 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 38 | 44 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 590 | 596 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 674 | 678 | PF02991 | 0.492 |
LIG_MYND_1 | 426 | 430 | PF01753 | 0.393 |
LIG_NRBOX | 197 | 203 | PF00104 | 0.361 |
LIG_REV1ctd_RIR_1 | 288 | 298 | PF16727 | 0.485 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.265 |
LIG_SH2_CRK | 375 | 379 | PF00017 | 0.446 |
LIG_SH2_CRK | 58 | 62 | PF00017 | 0.309 |
LIG_SH2_PTP2 | 143 | 146 | PF00017 | 0.246 |
LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.236 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.235 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.297 |
LIG_SH3_2 | 523 | 528 | PF14604 | 0.427 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.466 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.476 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.425 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.443 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.442 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.442 |
LIG_SUMO_SIM_anti_2 | 93 | 98 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 118 | 123 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 620 | 625 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 648 | 653 | PF11976 | 0.235 |
LIG_SUMO_SIM_par_1 | 687 | 692 | PF11976 | 0.270 |
LIG_TYR_ITIM | 228 | 233 | PF00017 | 0.259 |
LIG_TYR_ITIM | 56 | 61 | PF00017 | 0.270 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.270 |
LIG_WRC_WIRS_1 | 555 | 560 | PF05994 | 0.280 |
LIG_WW_3 | 308 | 312 | PF00397 | 0.464 |
MOD_CDK_SPxK_1 | 622 | 628 | PF00069 | 0.442 |
MOD_CDK_SPxxK_3 | 402 | 409 | PF00069 | 0.393 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.210 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.464 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.525 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.536 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.519 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.467 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.280 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.285 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.270 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.558 |
MOD_CK2_1 | 506 | 512 | PF00069 | 0.493 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.309 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.285 |
MOD_DYRK1A_RPxSP_1 | 382 | 386 | PF00069 | 0.411 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.321 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.286 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.452 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.264 |
MOD_GlcNHglycan | 296 | 300 | PF01048 | 0.285 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.306 |
MOD_GlcNHglycan | 36 | 40 | PF01048 | 0.254 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.354 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.279 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.326 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.500 |
MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.270 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.502 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.435 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.270 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.394 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.476 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.470 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.478 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.440 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.449 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.463 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.508 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.316 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.340 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.280 |
MOD_GSK3_1 | 685 | 692 | PF00069 | 0.274 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.302 |
MOD_N-GLC_1 | 11 | 16 | PF02516 | 0.477 |
MOD_N-GLC_1 | 391 | 396 | PF02516 | 0.330 |
MOD_N-GLC_1 | 566 | 571 | PF02516 | 0.442 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.292 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.364 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.283 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.333 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.465 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.548 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.371 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.258 |
MOD_NEK2_1 | 689 | 694 | PF00069 | 0.286 |
MOD_NEK2_2 | 487 | 492 | PF00069 | 0.437 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.367 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.285 |
MOD_PIKK_1 | 588 | 594 | PF00454 | 0.285 |
MOD_PIKK_1 | 650 | 656 | PF00454 | 0.270 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.246 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.277 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.464 |
MOD_Plk_1 | 369 | 375 | PF00069 | 0.484 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.469 |
MOD_Plk_2-3 | 272 | 278 | PF00069 | 0.418 |
MOD_Plk_2-3 | 352 | 358 | PF00069 | 0.583 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.324 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.235 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.281 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.360 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.468 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.454 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.280 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.270 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.367 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.280 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.277 |
MOD_Plk_4 | 696 | 702 | PF00069 | 0.326 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.549 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.429 |
MOD_ProDKin_1 | 422 | 428 | PF00069 | 0.407 |
MOD_ProDKin_1 | 500 | 506 | PF00069 | 0.474 |
MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.442 |
MOD_SUMO_rev_2 | 278 | 288 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 480 | 486 | PF00179 | 0.524 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 495 | 499 | PF00026 | 0.193 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8C5 | Leptomonas seymouri | 65% | 100% |
A0A1X0P0T2 | Trypanosomatidae | 53% | 100% |
A0A3S7X2A5 | Leishmania donovani | 94% | 100% |
A4HH72 | Leishmania braziliensis | 76% | 99% |
A4I4B8 | Leishmania infantum | 94% | 100% |
E9AM13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q63488 | Rattus norvegicus | 23% | 100% |
Q80UP8 | Mus musculus | 23% | 100% |
Q95L97 | Felis catus | 24% | 100% |