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 |
Related structures:
AlphaFold database: E9AXC8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.719 |
CLV_C14_Caspase3-7 | 404 | 408 | PF00656 | 0.727 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.845 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.769 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.845 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.769 |
CLV_PCSK_PC7_1 | 370 | 376 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.722 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.755 |
CLV_Separin_Metazoa | 462 | 466 | PF03568 | 0.659 |
DEG_APCC_DBOX_1 | 121 | 129 | PF00400 | 0.721 |
DEG_APCC_DBOX_1 | 324 | 332 | PF00400 | 0.631 |
DEG_APCC_DBOX_1 | 369 | 377 | PF00400 | 0.668 |
DEG_SCF_FBW7_2 | 426 | 432 | PF00400 | 0.517 |
DEG_SPOP_SBC_1 | 303 | 307 | PF00917 | 0.585 |
DEG_SPOP_SBC_1 | 493 | 497 | PF00917 | 0.672 |
DOC_CDC14_PxL_1 | 528 | 536 | PF14671 | 0.605 |
DOC_CKS1_1 | 25 | 30 | PF01111 | 0.615 |
DOC_CKS1_1 | 319 | 324 | PF01111 | 0.562 |
DOC_CKS1_1 | 426 | 431 | PF01111 | 0.514 |
DOC_CYCLIN_RxL_1 | 19 | 29 | PF00134 | 0.732 |
DOC_CYCLIN_RxL_1 | 362 | 369 | PF00134 | 0.658 |
DOC_MAPK_gen_1 | 374 | 381 | PF00069 | 0.674 |
DOC_MAPK_gen_1 | 516 | 524 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 550 | 558 | PF00069 | 0.602 |
DOC_PP1_RVXF_1 | 135 | 142 | PF00149 | 0.737 |
DOC_PP1_RVXF_1 | 238 | 245 | PF00149 | 0.638 |
DOC_PP2B_LxvP_1 | 174 | 177 | PF13499 | 0.775 |
DOC_PP2B_LxvP_1 | 424 | 427 | PF13499 | 0.694 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.703 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.727 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.835 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.812 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 137 | 142 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 14 | 21 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 143 | 148 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 181 | 185 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 197 | 202 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 390 | 400 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 502 | 511 | PF00244 | 0.694 |
LIG_Actin_WH2_2 | 167 | 183 | PF00022 | 0.483 |
LIG_BIR_III_2 | 359 | 363 | PF00653 | 0.698 |
LIG_BRCT_BRCA1_1 | 437 | 441 | PF00533 | 0.833 |
LIG_eIF4E_1 | 119 | 125 | PF01652 | 0.733 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.692 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.534 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.619 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.645 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.669 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.619 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.783 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.751 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.706 |
LIG_GBD_Chelix_1 | 120 | 128 | PF00786 | 0.724 |
LIG_Integrin_RGD_1 | 385 | 387 | PF01839 | 0.679 |
LIG_LIR_Gen_1 | 199 | 209 | PF02991 | 0.723 |
LIG_LIR_Gen_1 | 51 | 62 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.747 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.774 |
LIG_NRBOX | 338 | 344 | PF00104 | 0.617 |
LIG_NRBOX | 459 | 465 | PF00104 | 0.658 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.687 |
LIG_SH2_CRK | 329 | 333 | PF00017 | 0.571 |
LIG_SH2_SRC | 210 | 213 | PF00017 | 0.706 |
LIG_SH2_SRC | 259 | 262 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.729 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.746 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.616 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 520 | 523 | PF00017 | 0.666 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.833 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.757 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.743 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.596 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.489 |
LIG_SUMO_SIM_anti_2 | 264 | 269 | PF11976 | 0.671 |
LIG_SUMO_SIM_anti_2 | 55 | 61 | PF11976 | 0.643 |
LIG_SUMO_SIM_par_1 | 259 | 264 | PF11976 | 0.670 |
LIG_SUMO_SIM_par_1 | 520 | 525 | PF11976 | 0.592 |
LIG_TRAF2_1 | 446 | 449 | PF00917 | 0.720 |
LIG_TRFH_1 | 558 | 562 | PF08558 | 0.552 |
LIG_TYR_ITIM | 256 | 261 | PF00017 | 0.668 |
LIG_TYR_ITIM | 327 | 332 | PF00017 | 0.657 |
LIG_TYR_ITIM | 518 | 523 | PF00017 | 0.655 |
LIG_Vh1_VBS_1 | 65 | 83 | PF01044 | 0.471 |
LIG_WRC_WIRS_1 | 212 | 217 | PF05994 | 0.701 |
MOD_CDK_SPxxK_3 | 318 | 325 | PF00069 | 0.687 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.765 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.685 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.698 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.693 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.752 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.656 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.688 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.638 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.699 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.595 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.608 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.629 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.565 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.625 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.665 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.721 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.770 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.634 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.612 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.701 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.571 |
MOD_GlcNHglycan | 300 | 304 | PF01048 | 0.625 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.737 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.816 |
MOD_GlcNHglycan | 432 | 436 | PF01048 | 0.677 |
MOD_GlcNHglycan | 440 | 444 | PF01048 | 0.695 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.804 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.530 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.593 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.805 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.536 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.695 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.678 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.680 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.640 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.610 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.807 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.369 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.694 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.751 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.704 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.789 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.719 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.611 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.611 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.727 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.482 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.787 |
MOD_LATS_1 | 135 | 141 | PF00433 | 0.654 |
MOD_LATS_1 | 364 | 370 | PF00433 | 0.642 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.660 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.762 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.655 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.621 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.697 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.656 |
MOD_PKA_1 | 502 | 508 | PF00069 | 0.638 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.513 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.714 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.603 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.713 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.717 |
MOD_PKB_1 | 143 | 151 | PF00069 | 0.506 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.687 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.537 |
MOD_Plk_2-3 | 156 | 162 | PF00069 | 0.483 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.674 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.666 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.702 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.680 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.422 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.614 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.665 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.740 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.837 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.815 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.686 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.616 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.779 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.611 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.575 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.807 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.560 |
TRG_DiLeu_BaEn_1 | 335 | 340 | PF01217 | 0.668 |
TRG_DiLeu_BaEn_1 | 462 | 467 | PF01217 | 0.656 |
TRG_DiLeu_BaLyEn_6 | 363 | 368 | PF01217 | 0.740 |
TRG_DiLeu_LyEn_5 | 462 | 467 | PF01217 | 0.656 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.741 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.654 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.666 |
TRG_ER_diArg_1 | 142 | 145 | PF00400 | 0.780 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 373 | 375 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 516 | 518 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.756 |
TRG_NES_CRM1_1 | 416 | 430 | PF08389 | 0.561 |
TRG_NES_CRM1_1 | 458 | 472 | PF08389 | 0.669 |
TRG_NES_CRM1_1 | 87 | 100 | PF08389 | 0.748 |
TRG_Pf-PMV_PEXEL_1 | 465 | 469 | PF00026 | 0.667 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ID76 | Leishmania donovani | 84% | 100% |
A4HDZ3 | Leishmania braziliensis | 67% | 100% |
A4I192 | Leishmania infantum | 84% | 100% |
Q4QA44 | Leishmania major | 83% | 100% |