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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: E9AQR9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.422 |
CLV_PCSK_FUR_1 | 201 | 205 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 469 | 471 | PF00082 | 0.530 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.493 |
CLV_PCSK_PC7_1 | 73 | 79 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.393 |
DEG_APCC_DBOX_1 | 75 | 83 | PF00400 | 0.549 |
DEG_SCF_FBW7_1 | 151 | 156 | PF00400 | 0.526 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.530 |
DOC_CKS1_1 | 369 | 374 | PF01111 | 0.681 |
DOC_CKS1_1 | 376 | 381 | PF01111 | 0.807 |
DOC_MAPK_gen_1 | 110 | 119 | PF00069 | 0.422 |
DOC_PP4_FxxP_1 | 34 | 37 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 405 | 408 | PF00568 | 0.608 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.503 |
DOC_USP7_UBL2_3 | 167 | 171 | PF12436 | 0.591 |
DOC_USP7_UBL2_3 | 469 | 473 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.610 |
LIG_14-3-3_CanoR_1 | 36 | 42 | PF00244 | 0.557 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.581 |
LIG_BIR_III_2 | 52 | 56 | PF00653 | 0.507 |
LIG_BRCT_BRCA1_1 | 390 | 394 | PF00533 | 0.613 |
LIG_eIF4E_1 | 100 | 106 | PF01652 | 0.534 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.424 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.678 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.671 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.512 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.550 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.650 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.543 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.570 |
LIG_LIR_Apic_2 | 149 | 153 | PF02991 | 0.566 |
LIG_LIR_Apic_2 | 402 | 408 | PF02991 | 0.722 |
LIG_LIR_Gen_1 | 135 | 141 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 29 | 34 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.689 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.499 |
LIG_MYND_1 | 379 | 383 | PF01753 | 0.665 |
LIG_Pex14_1 | 401 | 405 | PF04695 | 0.598 |
LIG_Pex14_2 | 459 | 463 | PF04695 | 0.442 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.611 |
LIG_SH2_NCK_1 | 319 | 323 | PF00017 | 0.547 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.506 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.523 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.711 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.684 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.690 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.652 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.825 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.719 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.660 |
LIG_TRAF2_1 | 241 | 244 | PF00917 | 0.579 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.671 |
LIG_TRAF2_1 | 536 | 539 | PF00917 | 0.503 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.563 |
LIG_WW_2 | 350 | 353 | PF00397 | 0.545 |
MOD_CDK_SPxxK_3 | 368 | 375 | PF00069 | 0.678 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.609 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.521 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.668 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.719 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.541 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.567 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.651 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.411 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.507 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.574 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.573 |
MOD_DYRK1A_RPxSP_1 | 325 | 329 | PF00069 | 0.668 |
MOD_DYRK1A_RPxSP_1 | 368 | 372 | PF00069 | 0.673 |
MOD_DYRK1A_RPxSP_1 | 375 | 379 | PF00069 | 0.680 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.653 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.754 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.611 |
MOD_GlcNHglycan | 336 | 340 | PF01048 | 0.693 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.717 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.747 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.695 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.630 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.585 |
MOD_N-GLC_1 | 517 | 522 | PF02516 | 0.512 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.609 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.573 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.542 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.698 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.675 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.663 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.515 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.589 |
MOD_PIKK_1 | 517 | 523 | PF00454 | 0.512 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.589 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.583 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.539 |
MOD_Plk_1 | 517 | 523 | PF00069 | 0.512 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.586 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.541 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.582 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.503 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.530 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.707 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.682 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.735 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.607 |
TRG_DiLeu_BaEn_1 | 101 | 106 | PF01217 | 0.532 |
TRG_DiLeu_BaEn_4 | 49 | 55 | PF01217 | 0.648 |
TRG_DiLeu_BaEn_4 | 540 | 546 | PF01217 | 0.519 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.682 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.614 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 21 | 23 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.652 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.515 |
TRG_NLS_MonoExtC_3 | 109 | 115 | PF00514 | 0.411 |
TRG_NLS_MonoExtN_4 | 108 | 114 | PF00514 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 110 | 115 | PF00026 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICK9 | Leishmania donovani | 88% | 100% |
A4HX07 | Leishmania infantum | 87% | 100% |
Q4QEQ7 | Leishmania major | 88% | 100% |