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: A4HMS0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.535 |
CLV_PCSK_FUR_1 | 343 | 347 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.548 |
CLV_PCSK_PC7_1 | 275 | 281 | PF00082 | 0.439 |
CLV_PCSK_PC7_1 | 342 | 348 | PF00082 | 0.640 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.534 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.528 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.528 |
DOC_CYCLIN_RxL_1 | 296 | 304 | PF00134 | 0.396 |
DOC_CYCLIN_RxL_1 | 373 | 383 | PF00134 | 0.500 |
DOC_MAPK_DCC_7 | 8 | 16 | PF00069 | 0.441 |
DOC_MAPK_DCC_7 | 83 | 93 | PF00069 | 0.677 |
DOC_MAPK_gen_1 | 35 | 42 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 85 | 93 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 8 | 16 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 85 | 93 | PF00069 | 0.609 |
DOC_MAPK_RevD_3 | 91 | 107 | PF00069 | 0.694 |
DOC_PP1_RVXF_1 | 11 | 17 | PF00149 | 0.439 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.590 |
DOC_USP7_UBL2_3 | 100 | 104 | PF12436 | 0.549 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.644 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.570 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.600 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.514 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.345 |
DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.545 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.637 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.536 |
LIG_Actin_WH2_2 | 249 | 266 | PF00022 | 0.507 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.532 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.532 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.609 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.682 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.560 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.484 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.572 |
LIG_Integrin_RGD_1 | 195 | 197 | PF01839 | 0.531 |
LIG_LIR_Gen_1 | 349 | 360 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.490 |
LIG_MYND_1 | 219 | 223 | PF01753 | 0.502 |
LIG_Pex14_2 | 16 | 20 | PF04695 | 0.507 |
LIG_REV1ctd_RIR_1 | 250 | 258 | PF16727 | 0.433 |
LIG_SH2_PTP2 | 289 | 292 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.459 |
LIG_SH2_STAT3 | 356 | 359 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.430 |
LIG_SH3_3 | 315 | 321 | PF00018 | 0.547 |
LIG_SUMO_SIM_par_1 | 170 | 175 | PF11976 | 0.502 |
LIG_UBA3_1 | 10 | 18 | PF00899 | 0.598 |
LIG_WRC_WIRS_1 | 325 | 330 | PF05994 | 0.554 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.569 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.730 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.597 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.667 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.545 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.598 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.583 |
MOD_Cter_Amidation | 43 | 46 | PF01082 | 0.544 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.587 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.606 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.495 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.456 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.479 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.669 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.802 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.520 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.609 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.391 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.531 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.614 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.553 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.439 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.563 |
MOD_NEK2_2 | 99 | 104 | PF00069 | 0.461 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.588 |
MOD_PKA_1 | 118 | 124 | PF00069 | 0.573 |
MOD_PKA_1 | 346 | 352 | PF00069 | 0.634 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.389 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.481 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.459 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.520 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.675 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.540 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.613 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.532 |
MOD_PKB_1 | 346 | 354 | PF00069 | 0.582 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.543 |
MOD_SUMO_for_1 | 123 | 126 | PF00179 | 0.701 |
MOD_SUMO_rev_2 | 122 | 130 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 173 | 179 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 229 | 237 | PF00179 | 0.489 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.521 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 154 | 157 | PF00400 | 0.614 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 362 | 364 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.536 |
TRG_NLS_Bipartite_1 | 104 | 122 | PF00514 | 0.548 |
TRG_NLS_Bipartite_1 | 29 | 49 | PF00514 | 0.494 |
TRG_NLS_Bipartite_1 | 362 | 377 | PF00514 | 0.470 |
TRG_NLS_MonoCore_2 | 103 | 108 | PF00514 | 0.487 |
TRG_NLS_MonoCore_2 | 115 | 120 | PF00514 | 0.641 |
TRG_NLS_MonoExtC_3 | 104 | 109 | PF00514 | 0.531 |
TRG_NLS_MonoExtC_3 | 115 | 120 | PF00514 | 0.572 |
TRG_NLS_MonoExtC_3 | 20 | 25 | PF00514 | 0.554 |
TRG_NLS_MonoExtC_3 | 372 | 377 | PF00514 | 0.473 |
TRG_NLS_MonoExtN_4 | 104 | 109 | PF00514 | 0.483 |
TRG_NLS_MonoExtN_4 | 113 | 120 | PF00514 | 0.594 |
TRG_NLS_MonoExtN_4 | 18 | 25 | PF00514 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 109 | 114 | PF00026 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 379 | 383 | PF00026 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P943 | Leptomonas seymouri | 64% | 100% |
A0A3S7X9B6 | Leishmania donovani | 82% | 100% |
A4IBF6 | Leishmania infantum | 82% | 100% |
E9AF70 | Leishmania major | 80% | 100% |
E9B6C6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |