Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | no | yes: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 18 |
NetGPI | no | yes: 0, no: 18 |
Related structures:
AlphaFold database: A0A3S7WZC1
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 17 |
GO:0009987 | cellular process | 1 | 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0005488 | binding | 1 | 19 |
GO:0005515 | protein binding | 2 | 17 |
GO:0008270 | zinc ion binding | 6 | 9 |
GO:0030544 | Hsp70 protein binding | 4 | 17 |
GO:0031072 | heat shock protein binding | 3 | 17 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0046914 | transition metal ion binding | 5 | 9 |
GO:0051879 | Hsp90 protein binding | 4 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.324 |
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.286 |
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.429 |
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.579 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.548 |
CLV_PCSK_FUR_1 | 327 | 331 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 8 | 10 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.416 |
DOC_CYCLIN_RxL_1 | 160 | 172 | PF00134 | 0.519 |
DOC_MAPK_gen_1 | 62 | 70 | PF00069 | 0.320 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.579 |
DOC_USP7_UBL2_3 | 223 | 227 | PF12436 | 0.426 |
DOC_USP7_UBL2_3 | 241 | 245 | PF12436 | 0.438 |
LIG_14-3-3_CanoR_1 | 90 | 98 | PF00244 | 0.391 |
LIG_Actin_WH2_2 | 212 | 229 | PF00022 | 0.409 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.430 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.574 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.407 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.589 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.499 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.529 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.370 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.556 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.524 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 24 | 32 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 308 | 315 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 48 | 59 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.462 |
LIG_RPA_C_Fungi | 180 | 192 | PF08784 | 0.363 |
LIG_RPA_C_Fungi | 259 | 271 | PF08784 | 0.602 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.360 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.320 |
LIG_SH2_NCK_1 | 26 | 30 | PF00017 | 0.420 |
LIG_SH2_NCK_1 | 91 | 95 | PF00017 | 0.406 |
LIG_SH2_NCK_1 | 98 | 102 | PF00017 | 0.395 |
LIG_SH2_SRC | 111 | 114 | PF00017 | 0.359 |
LIG_SH2_SRC | 155 | 158 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.439 |
LIG_TRAF2_1 | 266 | 269 | PF00917 | 0.531 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.493 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.512 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.395 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.461 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.598 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.647 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.367 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.345 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.527 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.455 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.440 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.519 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.456 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.540 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.481 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.364 |
MOD_GlcNHglycan | 196 | 200 | PF01048 | 0.392 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.645 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.330 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.531 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.579 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.735 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.471 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.329 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.359 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.562 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.300 |
MOD_N-GLC_2 | 311 | 313 | PF02516 | 0.567 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.494 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.532 |
MOD_PKA_1 | 328 | 334 | PF00069 | 0.592 |
MOD_PKA_1 | 89 | 95 | PF00069 | 0.497 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.573 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.319 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.486 |
MOD_PKB_1 | 270 | 278 | PF00069 | 0.505 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.298 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.503 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.415 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.342 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.364 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.537 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.493 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.404 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.516 |
MOD_SUMO_rev_2 | 130 | 136 | PF00179 | 0.515 |
MOD_SUMO_rev_2 | 2 | 10 | PF00179 | 0.558 |
TRG_DiLeu_BaEn_1 | 177 | 182 | PF01217 | 0.519 |
TRG_DiLeu_BaLyEn_6 | 248 | 253 | PF01217 | 0.373 |
TRG_DiLeu_BaLyEn_6 | 321 | 326 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.406 |
TRG_ER_diArg_1 | 326 | 328 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.387 |
TRG_NLS_MonoExtC_3 | 327 | 332 | PF00514 | 0.552 |
TRG_NLS_MonoExtN_4 | 327 | 333 | PF00514 | 0.550 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTR8 | Leptomonas seymouri | 26% | 100% |
A0A0N1IBD2 | Leptomonas seymouri | 63% | 100% |
A0A0S4JRK3 | Bodo saltans | 35% | 95% |
A0A1X0NZH9 | Trypanosomatidae | 38% | 91% |
A0A3Q8IJP8 | Leishmania donovani | 24% | 100% |
A0A3R7LE97 | Trypanosoma rangeli | 41% | 94% |
A4HEB3 | Leishmania braziliensis | 84% | 100% |
A4HNL2 | Leishmania braziliensis | 24% | 100% |
A4I1Q9 | Leishmania infantum | 99% | 100% |
A4ICY0 | Leishmania infantum | 24% | 100% |
C9ZKB4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 96% |
E9ASC5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AXU3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q271 | Leishmania major | 25% | 100% |
Q4Q9M8 | Leishmania major | 95% | 100% |
V5BA34 | Trypanosoma cruzi | 25% | 100% |
V5BCJ3 | Trypanosoma cruzi | 41% | 94% |