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: A0A3S7X2K3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.704 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.566 |
CLV_PCSK_FUR_1 | 375 | 379 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 215 | 217 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 324 | 326 | PF00082 | 0.770 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.547 |
CLV_PCSK_PC7_1 | 375 | 381 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 66 | 72 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.480 |
CLV_Separin_Metazoa | 372 | 376 | PF03568 | 0.541 |
DOC_CYCLIN_RxL_1 | 10 | 24 | PF00134 | 0.377 |
DOC_CYCLIN_yCln2_LP_2 | 178 | 184 | PF00134 | 0.414 |
DOC_MAPK_gen_1 | 173 | 180 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 95 | 101 | PF00069 | 0.771 |
DOC_PP1_RVXF_1 | 14 | 21 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 178 | 181 | PF13499 | 0.481 |
DOC_PP4_FxxP_1 | 259 | 262 | PF00568 | 0.521 |
DOC_PP4_FxxP_1 | 41 | 44 | PF00568 | 0.517 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.695 |
DOC_USP7_UBL2_3 | 401 | 405 | PF12436 | 0.572 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.525 |
LIG_14-3-3_CanoR_1 | 325 | 333 | PF00244 | 0.804 |
LIG_14-3-3_CanoR_1 | 378 | 386 | PF00244 | 0.496 |
LIG_Actin_WH2_2 | 159 | 177 | PF00022 | 0.483 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.582 |
LIG_deltaCOP1_diTrp_1 | 283 | 289 | PF00928 | 0.550 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.427 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.730 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.447 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.422 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.585 |
LIG_HCF-1_HBM_1 | 392 | 395 | PF13415 | 0.540 |
LIG_LIR_Apic_2 | 256 | 262 | PF02991 | 0.507 |
LIG_LIR_Apic_2 | 40 | 44 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 283 | 289 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.476 |
LIG_Pex14_2 | 193 | 197 | PF04695 | 0.391 |
LIG_PTB_Apo_2 | 226 | 233 | PF02174 | 0.605 |
LIG_SH2_NCK_1 | 395 | 399 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 158 | 162 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.466 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.430 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.556 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.393 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.691 |
LIG_WRC_WIRS_1 | 286 | 291 | PF05994 | 0.557 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.721 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.599 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.536 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.767 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.738 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.458 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.411 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.570 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.632 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.747 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.535 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.720 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.700 |
MOD_GlcNHglycan | 313 | 317 | PF01048 | 0.675 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.697 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.682 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.582 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.551 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.715 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.720 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.524 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.680 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.341 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.622 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.730 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.764 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.500 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.563 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.757 |
MOD_NEK2_2 | 444 | 449 | PF00069 | 0.537 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.822 |
MOD_PKA_1 | 323 | 329 | PF00069 | 0.796 |
MOD_PKA_1 | 379 | 385 | PF00069 | 0.497 |
MOD_PKA_1 | 95 | 101 | PF00069 | 0.677 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.799 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.482 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.568 |
MOD_PKB_1 | 323 | 331 | PF00069 | 0.800 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.729 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.612 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.601 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.528 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.505 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.713 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.734 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.517 |
MOD_SUMO_for_1 | 347 | 350 | PF00179 | 0.509 |
MOD_SUMO_rev_2 | 212 | 217 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 319 | 326 | PF00179 | 0.784 |
TRG_DiLeu_BaEn_1 | 399 | 404 | PF01217 | 0.522 |
TRG_DiLeu_BaEn_1 | 78 | 83 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_2 | 414 | 420 | PF01217 | 0.613 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.552 |
TRG_ER_FFAT_1 | 414 | 425 | PF00635 | 0.439 |
TRG_NLS_Bipartite_1 | 367 | 382 | PF00514 | 0.403 |
TRG_NLS_MonoExtC_3 | 323 | 329 | PF00514 | 0.748 |
TRG_NLS_MonoExtC_3 | 377 | 383 | PF00514 | 0.504 |
TRG_NLS_MonoExtN_4 | 323 | 328 | PF00514 | 0.806 |
TRG_NLS_MonoExtN_4 | 375 | 382 | PF00514 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 70 | 75 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB34 | Leptomonas seymouri | 49% | 88% |
A0A0S4JH57 | Bodo saltans | 26% | 86% |
A0A1X0P158 | Trypanosomatidae | 31% | 100% |
A0A3R7MJJ2 | Trypanosoma rangeli | 31% | 100% |
A4HHJ1 | Leishmania braziliensis | 75% | 100% |
A4I4P9 | Leishmania infantum | 100% | 100% |
C9ZLD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AE52 | Leishmania major | 92% | 100% |
E9ALN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BGH3 | Trypanosoma cruzi | 30% | 100% |