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: 6 |
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Related structures:
AlphaFold database: E9AXU3
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 15 |
GO:0009987 | cellular process | 1 | 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0005488 | binding | 1 | 17 |
GO:0005515 | protein binding | 2 | 15 |
GO:0008270 | zinc ion binding | 6 | 9 |
GO:0030544 | Hsp70 protein binding | 4 | 15 |
GO:0031072 | heat shock protein binding | 3 | 15 |
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 | 15 |
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 | 0.317 |
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.419 |
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.506 |
CLV_PCSK_FUR_1 | 327 | 331 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 8 | 10 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.554 |
DOC_CYCLIN_RxL_1 | 160 | 172 | PF00134 | 0.492 |
DOC_MAPK_gen_1 | 62 | 70 | PF00069 | 0.372 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.387 |
DOC_USP7_UBL2_3 | 223 | 227 | PF12436 | 0.463 |
DOC_USP7_UBL2_3 | 241 | 245 | PF12436 | 0.520 |
LIG_14-3-3_CanoR_1 | 276 | 285 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 299 | 307 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 90 | 98 | PF00244 | 0.359 |
LIG_Actin_WH2_2 | 212 | 229 | PF00022 | 0.425 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.397 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.566 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.471 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.494 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.553 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.464 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.442 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.348 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.550 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.481 |
LIG_LIR_Gen_1 | 231 | 240 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 24 | 32 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 308 | 315 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 48 | 59 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.467 |
LIG_PTB_Apo_2 | 105 | 112 | PF02174 | 0.323 |
LIG_PTB_Phospho_1 | 105 | 111 | PF10480 | 0.323 |
LIG_RPA_C_Fungi | 180 | 192 | PF08784 | 0.320 |
LIG_RPA_C_Fungi | 259 | 271 | PF08784 | 0.569 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.374 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.282 |
LIG_SH2_NCK_1 | 26 | 30 | PF00017 | 0.316 |
LIG_SH2_NCK_1 | 91 | 95 | PF00017 | 0.372 |
LIG_SH2_NCK_1 | 98 | 102 | PF00017 | 0.364 |
LIG_SH2_SRC | 111 | 114 | PF00017 | 0.340 |
LIG_SH2_SRC | 155 | 158 | PF00017 | 0.354 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.398 |
LIG_TRAF2_1 | 266 | 269 | PF00917 | 0.489 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.461 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.510 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.349 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.386 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.559 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.634 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.344 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.329 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.335 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.500 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.417 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.337 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.474 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.414 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.539 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.353 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.318 |
MOD_GlcNHglycan | 196 | 200 | PF01048 | 0.348 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.385 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.614 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.283 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.499 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.635 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.729 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.170 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.477 |
MOD_LATS_1 | 274 | 280 | PF00433 | 0.418 |
MOD_N-GLC_1 | 183 | 188 | PF02516 | 0.315 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.532 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.276 |
MOD_N-GLC_2 | 311 | 313 | PF02516 | 0.536 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.484 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.436 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.532 |
MOD_PKA_1 | 328 | 334 | PF00069 | 0.546 |
MOD_PKA_1 | 89 | 95 | PF00069 | 0.293 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.530 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.331 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.613 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.544 |
MOD_PKB_1 | 270 | 278 | PF00069 | 0.470 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.483 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.413 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.334 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.324 |
MOD_Plk_2-3 | 33 | 39 | PF00069 | 0.170 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.441 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.550 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.506 |
MOD_SUMO_rev_2 | 130 | 136 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 2 | 10 | PF00179 | 0.540 |
TRG_DiLeu_BaEn_1 | 177 | 182 | PF01217 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 248 | 253 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 321 | 326 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 326 | 328 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.282 |
TRG_NLS_MonoExtC_3 | 327 | 332 | PF00514 | 0.509 |
TRG_NLS_MonoExtN_4 | 327 | 333 | PF00514 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTR8 | Leptomonas seymouri | 25% | 100% |
A0A0N1IBD2 | Leptomonas seymouri | 63% | 100% |
A0A0S4JRK3 | Bodo saltans | 34% | 95% |
A0A1X0NZH9 | Trypanosomatidae | 38% | 91% |
A0A3Q8IJP8 | Leishmania donovani | 22% | 100% |
A0A3R7LE97 | Trypanosoma rangeli | 41% | 94% |
A0A3S7WZC1 | Leishmania donovani | 95% | 100% |
A4HEB3 | Leishmania braziliensis | 85% | 100% |
A4I1Q9 | Leishmania infantum | 95% | 100% |
A4ICY0 | Leishmania infantum | 22% | 100% |
C9ZKB4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 96% |
E9ASC5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
Q4Q271 | Leishmania major | 23% | 100% |
Q4Q9M8 | Leishmania major | 95% | 100% |
V5BCJ3 | Trypanosoma cruzi | 41% | 94% |