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: E9B559
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 459 | 463 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.611 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.526 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.548 |
CLV_PCSK_FUR_1 | 330 | 334 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.606 |
CLV_PCSK_PC7_1 | 322 | 328 | PF00082 | 0.544 |
CLV_PCSK_PC7_1 | 443 | 449 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.594 |
DEG_APCC_DBOX_1 | 174 | 182 | PF00400 | 0.616 |
DEG_SCF_FBW7_1 | 65 | 72 | PF00400 | 0.581 |
DEG_SPOP_SBC_1 | 106 | 110 | PF00917 | 0.565 |
DEG_SPOP_SBC_1 | 455 | 459 | PF00917 | 0.497 |
DOC_CKS1_1 | 66 | 71 | PF01111 | 0.556 |
DOC_MAPK_FxFP_2 | 84 | 87 | PF00069 | 0.467 |
DOC_PP4_FxxP_1 | 242 | 245 | PF00568 | 0.486 |
DOC_PP4_FxxP_1 | 409 | 412 | PF00568 | 0.509 |
DOC_PP4_FxxP_1 | 53 | 56 | PF00568 | 0.689 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.580 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.674 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 169 | 177 | PF00244 | 0.793 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 552 | 561 | PF00244 | 0.584 |
LIG_BIR_III_2 | 519 | 523 | PF00653 | 0.576 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.528 |
LIG_CaM_IQ_9 | 314 | 329 | PF13499 | 0.570 |
LIG_CSL_BTD_1 | 498 | 501 | PF09270 | 0.585 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.496 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.657 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.640 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.767 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.636 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.611 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.657 |
LIG_LIR_Apic_2 | 240 | 245 | PF02991 | 0.570 |
LIG_LIR_Apic_2 | 246 | 251 | PF02991 | 0.633 |
LIG_LIR_Apic_2 | 63 | 69 | PF02991 | 0.577 |
LIG_LIR_Apic_2 | 82 | 87 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 299 | 308 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 364 | 370 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 450 | 461 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 533 | 540 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 68 | 78 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 450 | 456 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 533 | 538 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.530 |
LIG_MYND_1 | 83 | 87 | PF01753 | 0.466 |
LIG_Pex14_1 | 297 | 301 | PF04695 | 0.495 |
LIG_Pex14_1 | 304 | 308 | PF04695 | 0.481 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.611 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.498 |
LIG_SH2_CRK | 453 | 457 | PF00017 | 0.590 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.625 |
LIG_SH2_NCK_1 | 366 | 370 | PF00017 | 0.522 |
LIG_SH2_SRC | 366 | 369 | PF00017 | 0.594 |
LIG_SH2_STAP1 | 298 | 302 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 307 | 310 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 312 | 315 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.565 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.530 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.669 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.579 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.652 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.535 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.660 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.580 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.517 |
LIG_TRAF2_1 | 463 | 466 | PF00917 | 0.482 |
LIG_TYR_ITIM | 306 | 311 | PF00017 | 0.461 |
LIG_TYR_ITSM | 362 | 369 | PF00017 | 0.595 |
LIG_WW_3 | 262 | 266 | PF00397 | 0.655 |
MOD_CDC14_SPxK_1 | 411 | 414 | PF00782 | 0.665 |
MOD_CDC14_SPxK_1 | 64 | 67 | PF00782 | 0.605 |
MOD_CDK_SPK_2 | 421 | 426 | PF00069 | 0.681 |
MOD_CDK_SPxK_1 | 408 | 414 | PF00069 | 0.672 |
MOD_CDK_SPxK_1 | 61 | 67 | PF00069 | 0.619 |
MOD_CDK_SPxxK_3 | 335 | 342 | PF00069 | 0.578 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.721 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.566 |
MOD_CK1_1 | 186 | 192 | PF00069 | 0.796 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.685 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.628 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.682 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.616 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.590 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.609 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.562 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.820 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.641 |
MOD_Cter_Amidation | 327 | 330 | PF01082 | 0.622 |
MOD_DYRK1A_RPxSP_1 | 223 | 227 | PF00069 | 0.629 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.689 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.736 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.608 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.677 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.696 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.653 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.742 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.686 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.623 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.645 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.787 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.640 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.751 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.653 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.648 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.670 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.555 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.695 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.789 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.732 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.527 |
MOD_N-GLC_1 | 543 | 548 | PF02516 | 0.609 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.619 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.566 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.625 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.539 |
MOD_PIKK_1 | 419 | 425 | PF00454 | 0.623 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.537 |
MOD_PKA_1 | 332 | 338 | PF00069 | 0.656 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.608 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.579 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.656 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.551 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.631 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.613 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.723 |
MOD_PKB_1 | 180 | 188 | PF00069 | 0.637 |
MOD_PKB_1 | 541 | 549 | PF00069 | 0.565 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.606 |
MOD_Plk_2-3 | 168 | 174 | PF00069 | 0.636 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.458 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.642 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.625 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.725 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.604 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.619 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.573 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.574 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.641 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.592 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.584 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.602 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.612 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.497 |
MOD_SUMO_rev_2 | 445 | 454 | PF00179 | 0.408 |
TRG_DiLeu_BaEn_2 | 79 | 85 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_4 | 173 | 179 | PF01217 | 0.580 |
TRG_DiLeu_BaEn_4 | 466 | 472 | PF01217 | 0.493 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.606 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.589 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 327 | 330 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 404 | 407 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 494 | 497 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 566 | 569 | PF00400 | 0.685 |
TRG_ER_FFAT_2 | 411 | 422 | PF00635 | 0.514 |
TRG_NLS_MonoExtC_3 | 325 | 330 | PF00514 | 0.533 |
TRG_NLS_MonoExtN_4 | 324 | 330 | PF00514 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 223 | 228 | PF00026 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 39 | 44 | PF00026 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 447 | 451 | PF00026 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P607 | Leptomonas seymouri | 30% | 100% |
A0A3Q8IEH1 | Leishmania donovani | 80% | 100% |
A4HAY6 | Leishmania braziliensis | 59% | 97% |
A4IA45 | Leishmania infantum | 80% | 100% |
Q4Q2S6 | Leishmania major | 80% | 100% |