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:0005737 | cytoplasm | 2 | 12 |
GO:0005856 | cytoskeleton | 5 | 12 |
GO:0042995 | cell projection | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E9B1Q7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 167 | 171 | PF00656 | 0.661 |
CLV_C14_Caspase3-7 | 21 | 25 | PF00656 | 0.467 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 182 | 184 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.488 |
CLV_Separin_Metazoa | 144 | 148 | PF03568 | 0.534 |
DEG_APCC_DBOX_1 | 156 | 164 | PF00400 | 0.571 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.525 |
DOC_CYCLIN_RxL_1 | 26 | 33 | PF00134 | 0.284 |
DOC_CYCLIN_RxL_1 | 99 | 107 | PF00134 | 0.382 |
DOC_PP1_RVXF_1 | 128 | 134 | PF00149 | 0.453 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.498 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.577 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.399 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.749 |
LIG_14-3-3_CanoR_1 | 134 | 143 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 76 | 85 | PF00244 | 0.432 |
LIG_Actin_WH2_2 | 148 | 163 | PF00022 | 0.524 |
LIG_APCC_ABBA_1 | 187 | 192 | PF00400 | 0.617 |
LIG_BIR_III_2 | 24 | 28 | PF00653 | 0.479 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.474 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.369 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.550 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.426 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.655 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.643 |
LIG_LIR_Apic_2 | 103 | 108 | PF02991 | 0.491 |
LIG_LIR_Apic_2 | 175 | 179 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 137 | 146 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.354 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.512 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.464 |
LIG_SH2_CRK | 329 | 333 | PF00017 | 0.535 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.453 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.473 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.369 |
LIG_SH2_PTP2 | 364 | 367 | PF00017 | 0.453 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.479 |
LIG_SH2_SRC | 287 | 290 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.453 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.634 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.535 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.569 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.500 |
LIG_TYR_ITIM | 327 | 332 | PF00017 | 0.440 |
LIG_TYR_ITIM | 360 | 365 | PF00017 | 0.464 |
LIG_WRC_WIRS_1 | 56 | 61 | PF05994 | 0.599 |
MOD_CDK_SPxxK_3 | 104 | 111 | PF00069 | 0.400 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.287 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.654 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.433 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.677 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.527 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.495 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.655 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.604 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.434 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.434 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.540 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.392 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.363 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.230 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.643 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.620 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.545 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.242 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.528 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.558 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.583 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.608 |
MOD_N-GLC_2 | 361 | 363 | PF02516 | 0.253 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.326 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.530 |
MOD_NEK2_2 | 243 | 248 | PF00069 | 0.356 |
MOD_NEK2_2 | 344 | 349 | PF00069 | 0.550 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.541 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.433 |
MOD_PKB_1 | 49 | 57 | PF00069 | 0.509 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.544 |
MOD_Plk_2-3 | 164 | 170 | PF00069 | 0.700 |
MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.521 |
MOD_Plk_2-3 | 228 | 234 | PF00069 | 0.720 |
MOD_Plk_2-3 | 55 | 61 | PF00069 | 0.596 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.494 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.406 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.480 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.494 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.461 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.535 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.396 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.752 |
MOD_SUMO_rev_2 | 124 | 131 | PF00179 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 266 | 271 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 295 | 298 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.370 |
TRG_NES_CRM1_1 | 293 | 306 | PF08389 | 0.582 |
TRG_Pf-PMV_PEXEL_1 | 51 | 55 | PF00026 | 0.326 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P369 | Leptomonas seymouri | 51% | 100% |
A0A0S4JGK6 | Bodo saltans | 29% | 100% |
A0A1X0NJZ3 | Trypanosomatidae | 30% | 97% |
A0A3S7X4F5 | Leishmania donovani | 87% | 100% |
A0A422NQV4 | Trypanosoma rangeli | 37% | 100% |
A4HJ90 | Leishmania braziliensis | 78% | 100% |
A4I6N4 | Leishmania infantum | 87% | 100% |
C9ZM71 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
Q4Q6F3 | Leishmania major | 86% | 100% |
V5DGC7 | Trypanosoma cruzi | 39% | 96% |