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: A4HTA3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 233 | 237 | PF00656 | 0.698 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.768 |
CLV_C14_Caspase3-7 | 406 | 410 | PF00656 | 0.687 |
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.446 |
CLV_C14_Caspase3-7 | 585 | 589 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.476 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 600 | 602 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.430 |
DEG_COP1_1 | 329 | 339 | PF00400 | 0.715 |
DEG_SCF_FBW7_1 | 244 | 250 | PF00400 | 0.703 |
DEG_SCF_FBW7_1 | 85 | 92 | PF00400 | 0.678 |
DEG_SPOP_SBC_1 | 121 | 125 | PF00917 | 0.637 |
DEG_SPOP_SBC_1 | 235 | 239 | PF00917 | 0.824 |
DEG_SPOP_SBC_1 | 311 | 315 | PF00917 | 0.791 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.467 |
DOC_CKS1_1 | 244 | 249 | PF01111 | 0.705 |
DOC_CYCLIN_RxL_1 | 344 | 355 | PF00134 | 0.649 |
DOC_MAPK_MEF2A_6 | 558 | 567 | PF00069 | 0.406 |
DOC_MAPK_RevD_3 | 128 | 143 | PF00069 | 0.673 |
DOC_PP2B_LxvP_1 | 511 | 514 | PF13499 | 0.520 |
DOC_PP2B_LxvP_1 | 538 | 541 | PF13499 | 0.578 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.743 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.676 |
LIG_14-3-3_CanoR_1 | 106 | 113 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 133 | 141 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 17 | 25 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 438 | 444 | PF00244 | 0.732 |
LIG_14-3-3_CanoR_1 | 510 | 514 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 515 | 521 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 69 | 76 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 77 | 82 | PF00244 | 0.641 |
LIG_Actin_WH2_2 | 400 | 418 | PF00022 | 0.562 |
LIG_CSL_BTD_1 | 538 | 541 | PF09270 | 0.535 |
LIG_EH1_1 | 545 | 553 | PF00400 | 0.475 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.662 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.786 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.705 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.586 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.720 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.626 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.228 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.549 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.423 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.470 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.696 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.798 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.652 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.453 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.651 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.736 |
LIG_GBD_Chelix_1 | 563 | 571 | PF00786 | 0.470 |
LIG_LIR_Apic_2 | 536 | 542 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 206 | 216 | PF02991 | 0.661 |
LIG_LIR_Gen_1 | 338 | 346 | PF02991 | 0.670 |
LIG_LIR_Gen_1 | 395 | 405 | PF02991 | 0.682 |
LIG_LIR_Gen_1 | 545 | 552 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.668 |
LIG_LIR_Nem_3 | 338 | 342 | PF02991 | 0.679 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 457 | 462 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 545 | 549 | PF02991 | 0.564 |
LIG_Pex14_1 | 465 | 469 | PF04695 | 0.516 |
LIG_RPA_C_Fungi | 25 | 37 | PF08784 | 0.295 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.534 |
LIG_SH2_CRK | 371 | 375 | PF00017 | 0.601 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.642 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.669 |
LIG_SH2_NCK_1 | 258 | 262 | PF00017 | 0.690 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.690 |
LIG_SH2_STAP1 | 397 | 401 | PF00017 | 0.588 |
LIG_SH2_STAP1 | 559 | 563 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.591 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.713 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.571 |
LIG_SxIP_EBH_1 | 51 | 63 | PF03271 | 0.247 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.780 |
LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.677 |
LIG_WRC_WIRS_1 | 336 | 341 | PF05994 | 0.559 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.658 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.687 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.678 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.791 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.672 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.741 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.681 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.585 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.797 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.580 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.568 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.681 |
MOD_Cter_Amidation | 598 | 601 | PF01082 | 0.599 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.678 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.516 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.653 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.649 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.731 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.686 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.333 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.824 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.559 |
MOD_GlcNHglycan | 307 | 311 | PF01048 | 0.714 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.583 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.607 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.492 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.720 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.314 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.694 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.560 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.676 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.747 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.537 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.736 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.348 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.661 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.681 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.737 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.513 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.623 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.690 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.274 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.705 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.661 |
MOD_LATS_1 | 75 | 81 | PF00433 | 0.562 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.591 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.791 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.295 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.692 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.723 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.585 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.630 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.692 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.555 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.570 |
MOD_PIKK_1 | 198 | 204 | PF00454 | 0.727 |
MOD_PIKK_1 | 490 | 496 | PF00454 | 0.563 |
MOD_PK_1 | 77 | 83 | PF00069 | 0.563 |
MOD_PKA_1 | 69 | 75 | PF00069 | 0.540 |
MOD_PKA_1 | 77 | 83 | PF00069 | 0.538 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.538 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.622 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.228 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.690 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.681 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.733 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.597 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.563 |
MOD_PKB_1 | 15 | 23 | PF00069 | 0.590 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.592 |
MOD_Plk_2-3 | 319 | 325 | PF00069 | 0.754 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.690 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.486 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.717 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.630 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.670 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.705 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.647 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.646 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.585 |
MOD_SUMO_rev_2 | 319 | 327 | PF00179 | 0.783 |
TRG_DiLeu_BaEn_1 | 443 | 448 | PF01217 | 0.635 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.681 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.621 |
TRG_NES_CRM1_1 | 341 | 355 | PF08389 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.628 |
TRG_Pf-PMV_PEXEL_1 | 372 | 377 | PF00026 | 0.686 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WPX9 | Leishmania donovani | 100% | 100% |
A4H529 | Leishmania braziliensis | 71% | 100% |
E9AL92 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QIL2 | Leishmania major | 90% | 100% |