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: E9B3R9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.597 |
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.699 |
CLV_MEL_PAP_1 | 259 | 265 | PF00089 | 0.612 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.753 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.480 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.727 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.710 |
DEG_APCC_DBOX_1 | 205 | 213 | PF00400 | 0.492 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.615 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.633 |
DOC_CKS1_1 | 97 | 102 | PF01111 | 0.767 |
DOC_CYCLIN_RxL_1 | 203 | 210 | PF00134 | 0.482 |
DOC_CYCLIN_yCln2_LP_2 | 442 | 448 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 434 | 442 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.558 |
DOC_MAPK_RevD_3 | 440 | 454 | PF00069 | 0.447 |
DOC_PP1_RVXF_1 | 477 | 484 | PF00149 | 0.584 |
DOC_PP2B_LxvP_1 | 220 | 223 | PF13499 | 0.446 |
DOC_PP4_FxxP_1 | 337 | 340 | PF00568 | 0.695 |
DOC_PP4_FxxP_1 | 398 | 401 | PF00568 | 0.589 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.762 |
DOC_USP7_UBL2_3 | 322 | 326 | PF12436 | 0.702 |
DOC_USP7_UBL2_3 | 56 | 60 | PF12436 | 0.752 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.817 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.804 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 120 | 129 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 281 | 290 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 266 | 283 | PF00022 | 0.546 |
LIG_APCC_ABBA_1 | 232 | 237 | PF00400 | 0.592 |
LIG_APCC_ABBAyCdc20_2 | 479 | 485 | PF00400 | 0.478 |
LIG_EH_1 | 2 | 6 | PF12763 | 0.623 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.797 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.456 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.799 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.614 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.621 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.576 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.701 |
LIG_HCF-1_HBM_1 | 384 | 387 | PF13415 | 0.474 |
LIG_LIR_Apic_2 | 390 | 396 | PF02991 | 0.665 |
LIG_LIR_Apic_2 | 424 | 430 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.783 |
LIG_MYND_3 | 429 | 433 | PF01753 | 0.492 |
LIG_PTAP_UEV_1 | 75 | 80 | PF05743 | 0.513 |
LIG_Rb_pABgroove_1 | 437 | 445 | PF01858 | 0.584 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.453 |
LIG_SH2_CRK | 393 | 397 | PF00017 | 0.766 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.478 |
LIG_SH2_GRB2like | 484 | 487 | PF00017 | 0.477 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.580 |
LIG_SH2_SRC | 443 | 446 | PF00017 | 0.583 |
LIG_SH2_SRC | 484 | 487 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.686 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.788 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.629 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.780 |
LIG_SUMO_SIM_anti_2 | 447 | 452 | PF11976 | 0.465 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.819 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.586 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.636 |
MOD_CDK_SPxxK_3 | 79 | 86 | PF00069 | 0.717 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.790 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.718 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.620 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.573 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.765 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.745 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.782 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.659 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.800 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.593 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.686 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.640 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.607 |
MOD_Cter_Amidation | 259 | 262 | PF01082 | 0.594 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.758 |
MOD_GlcNHglycan | 178 | 182 | PF01048 | 0.647 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.660 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.740 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.692 |
MOD_GlcNHglycan | 415 | 419 | PF01048 | 0.717 |
MOD_GlcNHglycan | 69 | 73 | PF01048 | 0.614 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.542 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.796 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.802 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.681 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.422 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.592 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.771 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.708 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.763 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.673 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.662 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.546 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.503 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.799 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.613 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.495 |
MOD_PK_1 | 435 | 441 | PF00069 | 0.467 |
MOD_PKA_1 | 261 | 267 | PF00069 | 0.626 |
MOD_PKA_1 | 453 | 459 | PF00069 | 0.495 |
MOD_PKA_1 | 59 | 65 | PF00069 | 0.572 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.582 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.710 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.624 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.564 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.697 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.590 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.407 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.708 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.518 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.467 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.819 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.619 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.809 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.589 |
MOD_SUMO_for_1 | 321 | 324 | PF00179 | 0.735 |
MOD_SUMO_for_1 | 362 | 365 | PF00179 | 0.681 |
MOD_SUMO_for_1 | 412 | 415 | PF00179 | 0.723 |
MOD_SUMO_rev_2 | 288 | 298 | PF00179 | 0.643 |
MOD_SUMO_rev_2 | 428 | 437 | PF00179 | 0.455 |
TRG_DiLeu_BaLyEn_6 | 427 | 432 | PF01217 | 0.608 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 473 | 475 | PF00400 | 0.482 |
TRG_NLS_Bipartite_1 | 40 | 62 | PF00514 | 0.678 |
TRG_NLS_MonoExtC_3 | 118 | 124 | PF00514 | 0.826 |
TRG_NLS_MonoExtN_4 | 56 | 62 | PF00514 | 0.748 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 29 | 33 | PF00026 | 0.641 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBA2 | Leptomonas seymouri | 46% | 100% |
A0A3Q8ITX1 | Leishmania donovani | 91% | 100% |
A4HLE1 | Leishmania braziliensis | 75% | 99% |
A4I8V0 | Leishmania infantum | 91% | 100% |
Q4Q4A5 | Leishmania major | 89% | 100% |