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: E9B6C6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.461 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.661 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.599 |
CLV_PCSK_FUR_1 | 340 | 344 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.397 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 359 | 361 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 255 | 257 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 359 | 361 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.483 |
CLV_PCSK_PC7_1 | 272 | 278 | PF00082 | 0.439 |
CLV_PCSK_PC7_1 | 339 | 345 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.531 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.523 |
DOC_CYCLIN_RxL_1 | 293 | 301 | PF00134 | 0.397 |
DOC_CYCLIN_RxL_1 | 370 | 380 | PF00134 | 0.486 |
DOC_CYCLIN_yClb1_LxF_4 | 374 | 379 | PF00134 | 0.563 |
DOC_MAPK_DCC_7 | 81 | 91 | PF00069 | 0.669 |
DOC_MAPK_gen_1 | 370 | 379 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 83 | 91 | PF00069 | 0.600 |
DOC_MAPK_JIP1_4 | 373 | 379 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 83 | 91 | PF00069 | 0.600 |
DOC_MAPK_RevD_3 | 89 | 105 | PF00069 | 0.688 |
DOC_PP1_RVXF_1 | 374 | 380 | PF00149 | 0.563 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.569 |
DOC_USP7_UBL2_3 | 117 | 121 | PF12436 | 0.610 |
DOC_USP7_UBL2_3 | 125 | 129 | PF12436 | 0.550 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.596 |
DOC_USP7_UBL2_3 | 23 | 27 | PF12436 | 0.514 |
DOC_USP7_UBL2_3 | 251 | 255 | PF12436 | 0.413 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.561 |
DOC_USP7_UBL2_3 | 79 | 83 | PF12436 | 0.633 |
LIG_14-3-3_CanoR_1 | 344 | 350 | PF00244 | 0.534 |
LIG_Actin_WH2_2 | 246 | 263 | PF00022 | 0.508 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.530 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.723 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.591 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.559 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.607 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.692 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.558 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.481 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.576 |
LIG_Integrin_RGD_1 | 192 | 194 | PF01839 | 0.514 |
LIG_LIR_Gen_1 | 346 | 357 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 282 | 287 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 346 | 352 | PF02991 | 0.487 |
LIG_MYND_1 | 216 | 220 | PF01753 | 0.499 |
LIG_Pex14_2 | 16 | 20 | PF04695 | 0.500 |
LIG_REV1ctd_RIR_1 | 247 | 255 | PF16727 | 0.434 |
LIG_SH2_PTP2 | 286 | 289 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 353 | 356 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.433 |
LIG_UBA3_1 | 10 | 18 | PF00899 | 0.592 |
LIG_WRC_WIRS_1 | 322 | 327 | PF05994 | 0.540 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.672 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.628 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.551 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.603 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.383 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.577 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.551 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.625 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.498 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.453 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.675 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.675 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.692 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.584 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.545 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.544 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.608 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.388 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.615 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.349 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.501 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.540 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.435 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.551 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.594 |
MOD_PKA_1 | 116 | 122 | PF00069 | 0.545 |
MOD_PKA_1 | 343 | 349 | PF00069 | 0.633 |
MOD_PKA_1 | 359 | 365 | PF00069 | 0.387 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.689 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.564 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.610 |
MOD_PKB_1 | 343 | 351 | PF00069 | 0.580 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.572 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.539 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.570 |
MOD_SUMO_for_1 | 120 | 123 | PF00179 | 0.673 |
MOD_SUMO_rev_2 | 119 | 127 | PF00179 | 0.576 |
MOD_SUMO_rev_2 | 169 | 176 | PF00179 | 0.635 |
MOD_SUMO_rev_2 | 226 | 234 | PF00179 | 0.501 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.521 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 342 | 345 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.524 |
TRG_NLS_Bipartite_1 | 103 | 119 | PF00514 | 0.538 |
TRG_NLS_Bipartite_1 | 359 | 374 | PF00514 | 0.462 |
TRG_NLS_MonoCore_2 | 113 | 118 | PF00514 | 0.615 |
TRG_NLS_MonoExtC_3 | 102 | 107 | PF00514 | 0.527 |
TRG_NLS_MonoExtC_3 | 20 | 25 | PF00514 | 0.550 |
TRG_NLS_MonoExtC_3 | 369 | 374 | PF00514 | 0.461 |
TRG_NLS_MonoExtN_4 | 114 | 119 | PF00514 | 0.625 |
TRG_NLS_MonoExtN_4 | 18 | 25 | PF00514 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 376 | 380 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P943 | Leptomonas seymouri | 66% | 100% |
A0A3S7X9B6 | Leishmania donovani | 93% | 100% |
A4HMS0 | Leishmania braziliensis | 80% | 100% |
A4IBF6 | Leishmania infantum | 93% | 100% |
E9AF70 | Leishmania major | 89% | 100% |