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: E9AQ53
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.660 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.509 |
CLV_PCSK_FUR_1 | 244 | 248 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.681 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.534 |
DEG_APCC_DBOX_1 | 253 | 261 | PF00400 | 0.477 |
DEG_APCC_KENBOX_2 | 496 | 500 | PF00400 | 0.443 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.536 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.656 |
DEG_SPOP_SBC_1 | 195 | 199 | PF00917 | 0.686 |
DEG_SPOP_SBC_1 | 234 | 238 | PF00917 | 0.679 |
DOC_CYCLIN_yCln2_LP_2 | 210 | 216 | PF00134 | 0.582 |
DOC_MAPK_gen_1 | 169 | 178 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 3 | 12 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 32 | 42 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.490 |
DOC_PP1_RVXF_1 | 519 | 525 | PF00149 | 0.440 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.583 |
DOC_PP2B_LxvP_1 | 411 | 414 | PF13499 | 0.578 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.583 |
DOC_USP7_UBL2_3 | 179 | 183 | PF12436 | 0.459 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.653 |
DOC_USP7_UBL2_3 | 99 | 103 | PF12436 | 0.486 |
DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.515 |
LIG_14-3-3_CanoR_1 | 269 | 278 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 295 | 300 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 473 | 481 | PF00244 | 0.489 |
LIG_EVH1_2 | 418 | 422 | PF00568 | 0.458 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.543 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.669 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.366 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.523 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.522 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.578 |
LIG_LIR_Gen_1 | 425 | 433 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 425 | 430 | PF02991 | 0.560 |
LIG_PCNA_yPIPBox_3 | 112 | 121 | PF02747 | 0.466 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.445 |
LIG_SH3_2 | 415 | 420 | PF14604 | 0.561 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.676 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.529 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.616 |
LIG_SUMO_SIM_anti_2 | 173 | 180 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 173 | 180 | PF11976 | 0.431 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.537 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.450 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.621 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.586 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.504 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.588 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.628 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.431 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.582 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.714 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.660 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.583 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.618 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.557 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.573 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.600 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.580 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.532 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.495 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.598 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.470 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.705 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.686 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.558 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.437 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.580 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.746 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.631 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.479 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.619 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.714 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.502 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.430 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.579 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.427 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.592 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.555 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.387 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.493 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.573 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.542 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.523 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.570 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.477 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.533 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.463 |
MOD_PKB_1 | 505 | 513 | PF00069 | 0.437 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.488 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.448 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.568 |
MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.521 |
MOD_SUMO_for_1 | 299 | 302 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 124 | 134 | PF00179 | 0.562 |
TRG_DiLeu_BaEn_1 | 133 | 138 | PF01217 | 0.538 |
TRG_DiLeu_BaEn_1 | 173 | 178 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_4 | 173 | 179 | PF01217 | 0.529 |
TRG_DiLeu_LyEn_5 | 133 | 138 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.731 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.669 |
TRG_NLS_MonoExtC_3 | 502 | 507 | PF00514 | 0.430 |
TRG_NLS_MonoExtN_4 | 503 | 508 | PF00514 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 269 | 274 | PF00026 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.575 |
TRG_Pf-PMV_PEXEL_1 | 507 | 511 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I948 | Leptomonas seymouri | 44% | 86% |
A0A3Q8IA19 | Leishmania donovani | 88% | 99% |
A4H828 | Leishmania braziliensis | 70% | 100% |
A4HWF4 | Leishmania infantum | 87% | 99% |
Q4QFC9 | Leishmania major | 89% | 100% |