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 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HHJ1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.559 |
CLV_PCSK_FUR_1 | 390 | 394 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 392 | 394 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.757 |
CLV_PCSK_PC1ET2_1 | 392 | 394 | PF00082 | 0.538 |
CLV_PCSK_PC7_1 | 390 | 396 | PF00082 | 0.508 |
CLV_PCSK_PC7_1 | 66 | 72 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.498 |
CLV_Separin_Metazoa | 387 | 391 | PF03568 | 0.535 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.430 |
DEG_SCF_TRCP1_1 | 329 | 334 | PF00400 | 0.550 |
DEG_SPOP_SBC_1 | 140 | 144 | PF00917 | 0.343 |
DEG_SPOP_SBC_1 | 286 | 290 | PF00917 | 0.733 |
DOC_CYCLIN_RxL_1 | 10 | 24 | PF00134 | 0.382 |
DOC_MAPK_gen_1 | 305 | 312 | PF00069 | 0.437 |
DOC_PP1_RVXF_1 | 14 | 21 | PF00149 | 0.376 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.534 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.523 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.321 |
DOC_USP7_MATH_2 | 93 | 99 | PF00917 | 0.635 |
DOC_USP7_UBL2_3 | 416 | 420 | PF12436 | 0.591 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 340 | 348 | PF00244 | 0.789 |
LIG_14-3-3_CanoR_1 | 393 | 401 | PF00244 | 0.502 |
LIG_BIR_III_4 | 36 | 40 | PF00653 | 0.329 |
LIG_deltaCOP1_diTrp_1 | 297 | 303 | PF00928 | 0.566 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.491 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.425 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.363 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.633 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.630 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.437 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.418 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.470 |
LIG_GBD_Chelix_1 | 54 | 62 | PF00786 | 0.257 |
LIG_HCF-1_HBM_1 | 407 | 410 | PF13415 | 0.539 |
LIG_IRF3_LxIS_1 | 136 | 142 | PF10401 | 0.383 |
LIG_IRF3_LxIS_1 | 174 | 181 | PF10401 | 0.312 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.519 |
LIG_LIR_Apic_2 | 38 | 44 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 297 | 303 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 358 | 362 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 432 | 437 | PF02991 | 0.353 |
LIG_PDZ_Class_1 | 469 | 474 | PF00595 | 0.410 |
LIG_Pex14_1 | 239 | 243 | PF04695 | 0.368 |
LIG_PTB_Apo_2 | 9 | 16 | PF02174 | 0.310 |
LIG_SH2_NCK_1 | 410 | 414 | PF00017 | 0.561 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.463 |
LIG_SH3_2 | 91 | 96 | PF14604 | 0.469 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.425 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.405 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.511 |
LIG_SUMO_SIM_par_1 | 108 | 113 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 116 | 123 | PF11976 | 0.465 |
LIG_SxIP_EBH_1 | 96 | 110 | PF03271 | 0.493 |
LIG_WRC_WIRS_1 | 300 | 305 | PF05994 | 0.570 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.687 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.370 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.654 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.742 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.726 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.505 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.504 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.491 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.671 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.727 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.441 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.403 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.445 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.655 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.457 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.553 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.729 |
MOD_GlcNHglycan | 322 | 326 | PF01048 | 0.711 |
MOD_GlcNHglycan | 328 | 332 | PF01048 | 0.676 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.677 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.337 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.698 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.545 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.475 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.552 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.744 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.713 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.587 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.469 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.661 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.759 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.772 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.398 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.477 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.529 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.758 |
MOD_NEK2_2 | 459 | 464 | PF00069 | 0.523 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.528 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.811 |
MOD_PKA_1 | 394 | 400 | PF00069 | 0.490 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.775 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.526 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.567 |
MOD_PKB_1 | 340 | 348 | PF00069 | 0.764 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.550 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.641 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.542 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.508 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.535 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.649 |
MOD_SUMO_rev_2 | 223 | 228 | PF00179 | 0.561 |
MOD_SUMO_rev_2 | 334 | 341 | PF00179 | 0.768 |
TRG_DiLeu_BaEn_1 | 414 | 419 | PF01217 | 0.554 |
TRG_DiLeu_BaEn_1 | 78 | 83 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_2 | 429 | 435 | PF01217 | 0.604 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.542 |
TRG_NLS_MonoCore_2 | 391 | 396 | PF00514 | 0.350 |
TRG_NLS_MonoExtC_3 | 392 | 398 | PF00514 | 0.496 |
TRG_NLS_MonoExtN_4 | 338 | 343 | PF00514 | 0.791 |
TRG_NLS_MonoExtN_4 | 390 | 397 | PF00514 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 375 | 379 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 70 | 75 | PF00026 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB34 | Leptomonas seymouri | 49% | 91% |
A0A0S4JH57 | Bodo saltans | 29% | 89% |
A0A1X0P158 | Trypanosomatidae | 30% | 100% |
A0A3R7MJJ2 | Trypanosoma rangeli | 30% | 100% |
A0A3S7X2K3 | Leishmania donovani | 75% | 100% |
A4I4P9 | Leishmania infantum | 75% | 100% |
C9ZLD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AE52 | Leishmania major | 73% | 97% |
E9ALN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
V5BGH3 | Trypanosoma cruzi | 29% | 100% |