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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AE52
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.563 |
CLV_PCSK_FUR_1 | 375 | 379 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.519 |
CLV_PCSK_PC1ET2_1 | 324 | 326 | PF00082 | 0.771 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.547 |
CLV_PCSK_PC7_1 | 66 | 72 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.501 |
DOC_CYCLIN_RxL_1 | 10 | 24 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 173 | 180 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 95 | 101 | PF00069 | 0.677 |
DOC_PP1_RVXF_1 | 14 | 21 | PF00149 | 0.372 |
DOC_PP2B_LxvP_1 | 178 | 181 | PF13499 | 0.481 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.536 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.699 |
DOC_USP7_UBL2_3 | 401 | 405 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 325 | 333 | PF00244 | 0.802 |
LIG_14-3-3_CanoR_1 | 378 | 386 | PF00244 | 0.503 |
LIG_Actin_WH2_2 | 159 | 177 | PF00022 | 0.484 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.544 |
LIG_BIR_III_4 | 339 | 343 | PF00653 | 0.549 |
LIG_deltaCOP1_diTrp_1 | 283 | 289 | PF00928 | 0.557 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.417 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.525 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.427 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.729 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.549 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.447 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.418 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.469 |
LIG_HCF-1_HBM_1 | 392 | 395 | PF13415 | 0.537 |
LIG_LIR_Apic_2 | 256 | 262 | PF02991 | 0.518 |
LIG_LIR_Apic_2 | 40 | 44 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 240 | 251 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 283 | 291 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.488 |
LIG_Pex14_2 | 193 | 197 | PF04695 | 0.390 |
LIG_PTAP_UEV_1 | 180 | 185 | PF05743 | 0.374 |
LIG_PTB_Apo_2 | 226 | 233 | PF02174 | 0.510 |
LIG_SH2_CRK | 243 | 247 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 395 | 399 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.463 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.426 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.558 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.398 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.680 |
LIG_WRC_WIRS_1 | 286 | 291 | PF05994 | 0.563 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.740 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.593 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.522 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.762 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.745 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.685 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.451 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.404 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.444 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.696 |
MOD_GlcNHglycan | 267 | 271 | PF01048 | 0.761 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.549 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.693 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.743 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.582 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.728 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.727 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.720 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.524 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.655 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.590 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.743 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.776 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.767 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.476 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.531 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.757 |
MOD_NEK2_2 | 444 | 449 | PF00069 | 0.526 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.829 |
MOD_PKA_1 | 323 | 329 | PF00069 | 0.794 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.677 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.542 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.570 |
MOD_PKB_1 | 323 | 331 | PF00069 | 0.799 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.761 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.603 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.596 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.346 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.514 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.504 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.707 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.741 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.517 |
MOD_SUMO_rev_2 | 212 | 217 | PF00179 | 0.548 |
MOD_SUMO_rev_2 | 316 | 326 | PF00179 | 0.778 |
TRG_DiLeu_BaEn_1 | 399 | 404 | PF01217 | 0.554 |
TRG_DiLeu_BaEn_1 | 78 | 83 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_2 | 414 | 420 | PF01217 | 0.599 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.410 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.549 |
TRG_NES_CRM1_1 | 279 | 294 | PF08389 | 0.368 |
TRG_NLS_MonoExtC_3 | 323 | 329 | PF00514 | 0.746 |
TRG_NLS_MonoExtN_4 | 323 | 328 | PF00514 | 0.804 |
TRG_Pf-PMV_PEXEL_1 | 70 | 75 | PF00026 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB34 | Leptomonas seymouri | 48% | 88% |
A0A0S4JH57 | Bodo saltans | 27% | 86% |
A0A1X0P158 | Trypanosomatidae | 30% | 100% |
A0A3R7MJJ2 | Trypanosoma rangeli | 32% | 100% |
A0A3S7X2K3 | Leishmania donovani | 92% | 100% |
A4HHJ1 | Leishmania braziliensis | 73% | 97% |
A4I4P9 | Leishmania infantum | 92% | 100% |
C9ZLD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9ALN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BGH3 | Trypanosoma cruzi | 29% | 100% |