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: A0A3S5H7K0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.655 |
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.646 |
CLV_C14_Caspase3-7 | 397 | 401 | PF00656 | 0.598 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.689 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.709 |
CLV_PCSK_FUR_1 | 213 | 217 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.709 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.500 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.600 |
DEG_SPOP_SBC_1 | 175 | 179 | PF00917 | 0.602 |
DEG_SPOP_SBC_1 | 262 | 266 | PF00917 | 0.684 |
DEG_SPOP_SBC_1 | 374 | 378 | PF00917 | 0.690 |
DOC_CYCLIN_RxL_1 | 460 | 473 | PF00134 | 0.418 |
DOC_MAPK_gen_1 | 310 | 319 | PF00069 | 0.660 |
DOC_MAPK_gen_1 | 502 | 510 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 52 | 59 | PF00069 | 0.594 |
DOC_PP2B_PxIxI_1 | 451 | 457 | PF00149 | 0.499 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.799 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.532 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 75 | 80 | PF00244 | 0.704 |
LIG_APCC_ABBA_1 | 57 | 62 | PF00400 | 0.596 |
LIG_BIR_III_2 | 346 | 350 | PF00653 | 0.707 |
LIG_BIR_III_4 | 125 | 129 | PF00653 | 0.592 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.628 |
LIG_deltaCOP1_diTrp_1 | 411 | 418 | PF00928 | 0.606 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.655 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.586 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.543 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.593 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.613 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.706 |
LIG_FHA_2 | 316 | 322 | PF00498 | 0.557 |
LIG_FXI_DFP_1 | 415 | 419 | PF00024 | 0.702 |
LIG_Integrin_isoDGR_2 | 302 | 304 | PF01839 | 0.597 |
LIG_LIR_Gen_1 | 414 | 422 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.612 |
LIG_PDZ_Class_1 | 512 | 517 | PF00595 | 0.625 |
LIG_SH2_CRK | 497 | 501 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.665 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.598 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.707 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.632 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.740 |
LIG_SH3_3 | 473 | 479 | PF00018 | 0.572 |
LIG_SUMO_SIM_par_1 | 433 | 439 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 505 | 511 | PF11976 | 0.625 |
LIG_TRAF2_1 | 134 | 137 | PF00917 | 0.608 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.561 |
LIG_WW_3 | 49 | 53 | PF00397 | 0.720 |
MOD_CDK_SPK_2 | 228 | 233 | PF00069 | 0.690 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.645 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.790 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.767 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.681 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.607 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.654 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.718 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.553 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.612 |
MOD_Cter_Amidation | 73 | 76 | PF01082 | 0.717 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.585 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.629 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.661 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.700 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.652 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.711 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.682 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.763 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.511 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.679 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.691 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.699 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.551 |
MOD_NEK2_2 | 176 | 181 | PF00069 | 0.642 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.702 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.702 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.597 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.702 |
MOD_PKB_1 | 158 | 166 | PF00069 | 0.652 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.590 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.671 |
MOD_Plk_2-3 | 333 | 339 | PF00069 | 0.604 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.730 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.534 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.611 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.639 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.718 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.646 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.567 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.507 |
TRG_DiLeu_BaEn_1 | 194 | 199 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_2 | 456 | 462 | PF01217 | 0.422 |
TRG_DiLeu_BaEn_4 | 424 | 430 | PF01217 | 0.647 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 464 | 469 | PF01217 | 0.404 |
TRG_ENDOCYTIC_2 | 497 | 500 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.721 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 309 | 312 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.721 |
TRG_NLS_Bipartite_1 | 200 | 218 | PF00514 | 0.537 |
TRG_NLS_MonoExtC_3 | 213 | 218 | PF00514 | 0.587 |
TRG_NLS_MonoExtN_4 | 213 | 218 | PF00514 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 466 | 470 | PF00026 | 0.601 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA28 | Leptomonas seymouri | 43% | 100% |
A4HGV1 | Leishmania braziliensis | 64% | 98% |
A4I3Y1 | Leishmania infantum | 99% | 100% |
E9B071 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
Q4Q814 | Leishmania major | 85% | 99% |