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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: Q4Q592
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 2 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 2 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 331 | 335 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 575 | 579 | PF00656 | 0.514 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.729 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.755 |
CLV_PCSK_FUR_1 | 175 | 179 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.789 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.780 |
CLV_PCSK_PC1ET2_1 | 503 | 505 | PF00082 | 0.789 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.499 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.456 |
DEG_APCC_DBOX_1 | 342 | 350 | PF00400 | 0.452 |
DEG_MDM2_SWIB_1 | 28 | 36 | PF02201 | 0.466 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.665 |
DOC_CKS1_1 | 487 | 492 | PF01111 | 0.599 |
DOC_CKS1_1 | 597 | 602 | PF01111 | 0.487 |
DOC_CKS1_1 | 9 | 14 | PF01111 | 0.629 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 288 | 296 | PF00134 | 0.387 |
DOC_CYCLIN_yCln2_LP_2 | 580 | 586 | PF00134 | 0.556 |
DOC_MAPK_gen_1 | 269 | 277 | PF00069 | 0.378 |
DOC_MAPK_HePTP_8 | 91 | 103 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 272 | 279 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 88 | 95 | PF00069 | 0.602 |
DOC_MAPK_NFAT4_5 | 272 | 280 | PF00069 | 0.462 |
DOC_PP2B_LxvP_1 | 536 | 539 | PF13499 | 0.457 |
DOC_PP4_FxxP_1 | 189 | 192 | PF00568 | 0.784 |
DOC_PP4_FxxP_1 | 487 | 490 | PF00568 | 0.622 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.398 |
LIG_Actin_WH2_2 | 129 | 145 | PF00022 | 0.416 |
LIG_Actin_WH2_2 | 315 | 330 | PF00022 | 0.282 |
LIG_APCC_ABBA_1 | 598 | 603 | PF00400 | 0.558 |
LIG_BRCT_BRCA1_1 | 121 | 125 | PF00533 | 0.399 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.483 |
LIG_BRCT_BRCA1_1 | 40 | 44 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.599 |
LIG_BRCT_BRCA1_1 | 441 | 445 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 494 | 498 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.363 |
LIG_CaM_NSCaTE_8 | 374 | 381 | PF13499 | 0.496 |
LIG_EH_1 | 122 | 126 | PF12763 | 0.344 |
LIG_EVH1_1 | 487 | 491 | PF00568 | 0.622 |
LIG_EVH1_2 | 594 | 598 | PF00568 | 0.558 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.670 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.431 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.477 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.456 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.554 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.199 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.483 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.483 |
LIG_FHA_2 | 570 | 576 | PF00498 | 0.510 |
LIG_Integrin_isoDGR_2 | 270 | 272 | PF01839 | 0.639 |
LIG_LIR_Apic_2 | 187 | 192 | PF02991 | 0.782 |
LIG_LIR_Gen_1 | 351 | 360 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 619 | 625 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 351 | 355 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 540 | 545 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 619 | 625 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.483 |
LIG_MLH1_MIPbox_1 | 34 | 38 | PF16413 | 0.416 |
LIG_NRBOX | 164 | 170 | PF00104 | 0.620 |
LIG_NRBOX | 4 | 10 | PF00104 | 0.526 |
LIG_PDZ_Class_3 | 620 | 625 | PF00595 | 0.574 |
LIG_Pex14_1 | 258 | 262 | PF04695 | 0.363 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.736 |
LIG_Pex14_2 | 28 | 32 | PF04695 | 0.483 |
LIG_PTB_Apo_2 | 120 | 127 | PF02174 | 0.419 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 527 | 531 | PF00017 | 0.558 |
LIG_SH2_PTP2 | 352 | 355 | PF00017 | 0.442 |
LIG_SH2_SRC | 263 | 266 | PF00017 | 0.420 |
LIG_SH2_SRC | 352 | 355 | PF00017 | 0.442 |
LIG_SH2_SRC | 622 | 625 | PF00017 | 0.576 |
LIG_SH2_STAT3 | 463 | 466 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.474 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.427 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.620 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.608 |
LIG_SH3_3 | 588 | 594 | PF00018 | 0.555 |
LIG_SUMO_SIM_anti_2 | 240 | 249 | PF11976 | 0.503 |
LIG_SUMO_SIM_anti_2 | 273 | 279 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 240 | 249 | PF11976 | 0.534 |
LIG_SUMO_SIM_par_1 | 51 | 57 | PF11976 | 0.483 |
LIG_TRFH_1 | 229 | 233 | PF08558 | 0.483 |
LIG_TYR_ITIM | 261 | 266 | PF00017 | 0.437 |
LIG_UBA3_1 | 274 | 281 | PF00899 | 0.463 |
MOD_CDK_SPxK_1 | 596 | 602 | PF00069 | 0.557 |
MOD_CDK_SPxK_1 | 8 | 14 | PF00069 | 0.626 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.817 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.499 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.540 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.560 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.580 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.483 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.506 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.450 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.603 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.397 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.383 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.666 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.806 |
MOD_GlcNHglycan | 499 | 503 | PF01048 | 0.780 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.709 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.664 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.660 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.774 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.483 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.682 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.675 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.316 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.420 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.590 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.520 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.627 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.574 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.576 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.621 |
MOD_N-GLC_1 | 530 | 535 | PF02516 | 0.715 |
MOD_N-GLC_2 | 280 | 282 | PF02516 | 0.631 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.366 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.640 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.610 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.566 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.477 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.458 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.379 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.493 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.278 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.483 |
MOD_NEK2_2 | 215 | 220 | PF00069 | 0.747 |
MOD_NEK2_2 | 32 | 37 | PF00069 | 0.402 |
MOD_NEK2_2 | 576 | 581 | PF00069 | 0.561 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.483 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.755 |
MOD_PIKK_1 | 221 | 227 | PF00454 | 0.649 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.338 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.521 |
MOD_PIKK_1 | 73 | 79 | PF00454 | 0.667 |
MOD_PK_1 | 453 | 459 | PF00069 | 0.510 |
MOD_PKA_1 | 439 | 445 | PF00069 | 0.524 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.438 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.704 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.583 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.540 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.545 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.602 |
MOD_PKB_1 | 326 | 334 | PF00069 | 0.426 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.405 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.508 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.227 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.410 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.442 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.337 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.452 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.495 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.602 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.423 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.602 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.369 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.750 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.690 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.549 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.585 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.471 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.594 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.557 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.626 |
TRG_DiLeu_BaEn_1 | 320 | 325 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_1 | 4 | 9 | PF01217 | 0.619 |
TRG_DiLeu_BaLyEn_6 | 325 | 330 | PF01217 | 0.277 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 622 | 625 | PF00928 | 0.576 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 325 | 328 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 612 | 614 | PF00400 | 0.555 |
TRG_ER_FFAT_2 | 187 | 194 | PF00635 | 0.736 |
TRG_NES_CRM1_1 | 138 | 149 | PF08389 | 0.483 |
TRG_NES_CRM1_1 | 345 | 356 | PF08389 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 344 | 348 | PF00026 | 0.640 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X5K5 | Leishmania donovani | 89% | 100% |
A4HKH5 | Leishmania braziliensis | 60% | 100% |
A4I802 | Leishmania infantum | 88% | 100% |
E9B2W4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |