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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A0A3S7X8N2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 79 | 83 | PF00656 | 0.583 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.624 |
CLV_PCSK_FUR_1 | 102 | 106 | PF00082 | 0.634 |
CLV_PCSK_FUR_1 | 502 | 506 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.697 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.497 |
CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.577 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 479 | 481 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.487 |
CLV_PCSK_PC7_1 | 100 | 106 | PF00082 | 0.528 |
CLV_PCSK_PC7_1 | 343 | 349 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.559 |
CLV_Separin_Metazoa | 344 | 348 | PF03568 | 0.672 |
DEG_APCC_DBOX_1 | 504 | 512 | PF00400 | 0.454 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.611 |
DOC_CYCLIN_RxL_1 | 262 | 269 | PF00134 | 0.495 |
DOC_CYCLIN_RxL_1 | 502 | 513 | PF00134 | 0.368 |
DOC_CYCLIN_yCln2_LP_2 | 311 | 317 | PF00134 | 0.634 |
DOC_MAPK_gen_1 | 502 | 511 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 444 | 453 | PF00069 | 0.703 |
DOC_MAPK_RevD_3 | 285 | 300 | PF00069 | 0.576 |
DOC_PP1_RVXF_1 | 152 | 159 | PF00149 | 0.508 |
DOC_PP2B_LxvP_1 | 226 | 229 | PF13499 | 0.580 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 450 | 454 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 123 | 132 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 237 | 244 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.608 |
LIG_14-3-3_CterR_2 | 553 | 555 | PF00244 | 0.627 |
LIG_DLG_GKlike_1 | 170 | 177 | PF00625 | 0.595 |
LIG_EH1_1 | 46 | 54 | PF00400 | 0.595 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.696 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.595 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.507 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.545 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.593 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.663 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.497 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.640 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.434 |
LIG_FHA_2 | 28 | 34 | PF00498 | 0.604 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.562 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.431 |
LIG_Integrin_RGD_1 | 70 | 72 | PF01839 | 0.611 |
LIG_LIR_Gen_1 | 544 | 549 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 544 | 548 | PF02991 | 0.500 |
LIG_MYND_1 | 314 | 318 | PF01753 | 0.631 |
LIG_NRBOX | 263 | 269 | PF00104 | 0.563 |
LIG_RPA_C_Fungi | 252 | 264 | PF08784 | 0.582 |
LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.682 |
LIG_SH2_STAT3 | 531 | 534 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.697 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.573 |
LIG_Sin3_3 | 285 | 292 | PF02671 | 0.562 |
LIG_Sin3_3 | 353 | 360 | PF02671 | 0.560 |
LIG_SUMO_SIM_par_1 | 21 | 26 | PF11976 | 0.638 |
LIG_SUMO_SIM_par_1 | 283 | 290 | PF11976 | 0.479 |
LIG_TRAF2_1 | 233 | 236 | PF00917 | 0.630 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.447 |
LIG_UBA3_1 | 470 | 479 | PF00899 | 0.593 |
LIG_WRC_WIRS_1 | 160 | 165 | PF05994 | 0.521 |
LIG_WW_3 | 62 | 66 | PF00397 | 0.631 |
MOD_CDK_SPK_2 | 185 | 190 | PF00069 | 0.532 |
MOD_CDK_SPxxK_3 | 185 | 192 | PF00069 | 0.529 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.556 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.521 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.622 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.587 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.599 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.555 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.641 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.534 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.537 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.523 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.616 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.587 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.429 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.584 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.445 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.664 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.457 |
MOD_GlcNHglycan | 24 | 28 | PF01048 | 0.548 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.700 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.615 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.568 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.568 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.604 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.608 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.497 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.521 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.570 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.574 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.554 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.604 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.622 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.514 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.455 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.586 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.497 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.527 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.490 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.519 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.500 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.609 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.579 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.537 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.577 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.557 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.595 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.590 |
MOD_PKA_1 | 104 | 110 | PF00069 | 0.605 |
MOD_PKA_1 | 370 | 376 | PF00069 | 0.555 |
MOD_PKA_1 | 391 | 397 | PF00069 | 0.560 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.605 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.629 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.459 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.534 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.555 |
MOD_PKA_2 | 391 | 397 | PF00069 | 0.697 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.667 |
MOD_PKB_1 | 102 | 110 | PF00069 | 0.620 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.648 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.492 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.570 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.500 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.593 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.675 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.493 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.542 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.667 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.549 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.510 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.653 |
MOD_SUMO_rev_2 | 443 | 451 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 50 | 59 | PF00179 | 0.595 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 164 | 169 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 226 | 231 | PF01217 | 0.525 |
TRG_DiLeu_BaLyEn_6 | 419 | 424 | PF01217 | 0.529 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 420 | 423 | PF00400 | 0.537 |
TRG_NLS_MonoExtC_3 | 477 | 482 | PF00514 | 0.603 |
TRG_NLS_MonoExtN_4 | 476 | 483 | PF00514 | 0.618 |
TRG_NLS_MonoExtN_4 | 502 | 508 | PF00514 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2P1 | Leptomonas seymouri | 43% | 99% |
A4HBG7 | Leishmania braziliensis | 74% | 100% |
A4IAL3 | Leishmania infantum | 99% | 100% |
E9B5N8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q280 | Leishmania major | 87% | 100% |