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: E9AYF4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 127 | 131 | PF00656 | 0.832 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.725 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.827 |
CLV_PCSK_FUR_1 | 189 | 193 | PF00082 | 0.618 |
CLV_PCSK_FUR_1 | 249 | 253 | PF00082 | 0.616 |
CLV_PCSK_FUR_1 | 362 | 366 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.741 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 456 | 458 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.827 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 364 | 366 | PF00082 | 0.674 |
CLV_PCSK_PC1ET2_1 | 456 | 458 | PF00082 | 0.704 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.727 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.710 |
DEG_APCC_DBOX_1 | 301 | 309 | PF00400 | 0.543 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.751 |
DOC_CKS1_1 | 142 | 147 | PF01111 | 0.674 |
DOC_CKS1_1 | 350 | 355 | PF01111 | 0.673 |
DOC_CYCLIN_RxL_1 | 369 | 382 | PF00134 | 0.654 |
DOC_MAPK_gen_1 | 300 | 307 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 367 | 379 | PF00069 | 0.665 |
DOC_MAPK_MEF2A_6 | 270 | 279 | PF00069 | 0.641 |
DOC_MAPK_RevD_3 | 2 | 16 | PF00069 | 0.623 |
DOC_PP1_RVXF_1 | 412 | 418 | PF00149 | 0.629 |
DOC_PP4_MxPP_1 | 433 | 436 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.653 |
DOC_USP7_UBL2_3 | 473 | 477 | PF12436 | 0.765 |
DOC_WW_Pin1_4 | 135 | 140 | PF00397 | 0.797 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.783 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 169 | 179 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 21 | 29 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 234 | 243 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 302 | 308 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 369 | 379 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 52 | 58 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 79 | 88 | PF00244 | 0.707 |
LIG_Actin_RPEL_3 | 358 | 377 | PF02755 | 0.600 |
LIG_APCC_ABBA_1 | 377 | 382 | PF00400 | 0.638 |
LIG_BRCT_BRCA1_1 | 322 | 326 | PF00533 | 0.636 |
LIG_BRCT_BRCA1_1 | 41 | 45 | PF00533 | 0.774 |
LIG_CaM_IQ_9 | 221 | 236 | PF13499 | 0.579 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.555 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.729 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.402 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.439 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.663 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.554 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.805 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.734 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.647 |
LIG_LIR_Gen_1 | 144 | 153 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 306 | 315 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.601 |
LIG_NRBOX | 314 | 320 | PF00104 | 0.336 |
LIG_Pex14_2 | 326 | 330 | PF04695 | 0.648 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.622 |
LIG_SH2_PTP2 | 424 | 427 | PF00017 | 0.623 |
LIG_SH2_SRC | 128 | 131 | PF00017 | 0.652 |
LIG_SH2_STAT3 | 245 | 248 | PF00017 | 0.567 |
LIG_SH2_STAT3 | 258 | 261 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.595 |
LIG_SH3_1 | 432 | 438 | PF00018 | 0.695 |
LIG_SH3_2 | 136 | 141 | PF14604 | 0.739 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.802 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.561 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.695 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.810 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.546 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.804 |
LIG_TRAF2_1 | 331 | 334 | PF00917 | 0.463 |
LIG_WW_3 | 57 | 61 | PF00397 | 0.512 |
MOD_CDC14_SPxK_1 | 138 | 141 | PF00782 | 0.737 |
MOD_CDK_SPK_2 | 135 | 140 | PF00069 | 0.742 |
MOD_CDK_SPxK_1 | 135 | 141 | PF00069 | 0.742 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.594 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.834 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.665 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.541 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.659 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.717 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.590 |
MOD_Cter_Amidation | 13 | 16 | PF01082 | 0.646 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.622 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.575 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.706 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.589 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.671 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.635 |
MOD_GlcNHglycan | 40 | 44 | PF01048 | 0.725 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.679 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.680 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.674 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.624 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.668 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.510 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.639 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.781 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.399 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.579 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.527 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.564 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.477 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.545 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.756 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.687 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.506 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.648 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.476 |
MOD_NEK2_2 | 396 | 401 | PF00069 | 0.649 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.619 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.734 |
MOD_PKA_1 | 140 | 146 | PF00069 | 0.709 |
MOD_PKA_1 | 16 | 22 | PF00069 | 0.836 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.547 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.605 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.800 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.547 |
MOD_PKB_1 | 232 | 240 | PF00069 | 0.685 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.682 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.514 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.653 |
MOD_ProDKin_1 | 135 | 141 | PF00069 | 0.796 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.676 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.785 |
MOD_SUMO_rev_2 | 333 | 339 | PF00179 | 0.654 |
MOD_SUMO_rev_2 | 445 | 451 | PF00179 | 0.673 |
TRG_DiLeu_BaEn_1 | 205 | 210 | PF01217 | 0.504 |
TRG_DiLeu_BaEn_1 | 314 | 319 | PF01217 | 0.549 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.615 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.623 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.724 |
TRG_ER_diArg_1 | 189 | 192 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 231 | 234 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 273 | 276 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.825 |
TRG_ER_diLys_1 | 473 | 477 | PF00400 | 0.765 |
TRG_Pf-PMV_PEXEL_1 | 207 | 212 | PF00026 | 0.646 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.648 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IC93 | Leishmania donovani | 89% | 100% |
A4HD53 | Leishmania braziliensis | 68% | 99% |
A4I2A8 | Leishmania infantum | 89% | 100% |
Q4Q917 | Leishmania major | 89% | 100% |