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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9ALH2
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.429 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.566 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.329 |
CLV_PCSK_FUR_1 | 183 | 187 | PF00082 | 0.417 |
CLV_PCSK_FUR_1 | 352 | 356 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.360 |
DEG_SPOP_SBC_1 | 154 | 158 | PF00917 | 0.499 |
DEG_SPOP_SBC_1 | 321 | 325 | PF00917 | 0.536 |
DOC_CKS1_1 | 137 | 142 | PF01111 | 0.487 |
DOC_CKS1_1 | 216 | 221 | PF01111 | 0.502 |
DOC_CKS1_1 | 237 | 242 | PF01111 | 0.473 |
DOC_CKS1_1 | 371 | 376 | PF01111 | 0.672 |
DOC_CYCLIN_yCln2_LP_2 | 216 | 222 | PF00134 | 0.494 |
DOC_MAPK_gen_1 | 255 | 264 | PF00069 | 0.458 |
DOC_MAPK_gen_1 | 388 | 394 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 255 | 264 | PF00069 | 0.479 |
DOC_PP2B_LxvP_1 | 66 | 69 | PF13499 | 0.527 |
DOC_PP4_FxxP_1 | 137 | 140 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.256 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.500 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.407 |
LIG_14-3-3_CanoR_1 | 102 | 106 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 20 | 28 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 346 | 351 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 354 | 364 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.216 |
LIG_AP2alpha_2 | 221 | 223 | PF02296 | 0.451 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.668 |
LIG_BIR_III_2 | 328 | 332 | PF00653 | 0.518 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.309 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.432 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.525 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.489 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.485 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.615 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.430 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.511 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.536 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.556 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.336 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.537 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.500 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.472 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.532 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.662 |
LIG_LIR_Gen_1 | 104 | 113 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 12 | 19 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 62 | 72 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 12 | 16 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.579 |
LIG_NRBOX | 190 | 196 | PF00104 | 0.490 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.400 |
LIG_SH2_CRK | 32 | 36 | PF00017 | 0.255 |
LIG_SH2_NCK_1 | 107 | 111 | PF00017 | 0.558 |
LIG_SH2_NCK_1 | 313 | 317 | PF00017 | 0.486 |
LIG_SH2_SRC | 105 | 108 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.486 |
LIG_SH2_STAT3 | 190 | 193 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.588 |
LIG_SH3_2 | 371 | 376 | PF14604 | 0.721 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.554 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.504 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.491 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.790 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.634 |
LIG_SUMO_SIM_anti_2 | 347 | 352 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 156 | 163 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 208 | 215 | PF11976 | 0.416 |
LIG_TRAF2_1 | 358 | 361 | PF00917 | 0.602 |
LIG_WRC_WIRS_1 | 267 | 272 | PF05994 | 0.319 |
MOD_CDK_SPxK_1 | 236 | 242 | PF00069 | 0.478 |
MOD_CDK_SPxK_1 | 370 | 376 | PF00069 | 0.715 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.593 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.532 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.683 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.461 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.417 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.635 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.738 |
MOD_Cter_Amidation | 352 | 355 | PF01082 | 0.528 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.615 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.540 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.663 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.707 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.348 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.523 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.591 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.590 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.439 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.549 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.462 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.404 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.599 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.491 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.584 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.690 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.624 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.465 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.427 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.657 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.479 |
MOD_NEK2_2 | 117 | 122 | PF00069 | 0.607 |
MOD_NEK2_2 | 291 | 296 | PF00069 | 0.472 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.408 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.408 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.289 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.191 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.485 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.546 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.579 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.320 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.477 |
MOD_Plk_1 | 228 | 234 | PF00069 | 0.613 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.620 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.414 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.294 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.368 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.317 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.403 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.551 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.620 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.478 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.704 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.398 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.588 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.380 |
TRG_ER_diArg_1 | 19 | 21 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.490 |
TRG_ER_diArg_1 | 390 | 392 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.347 |
TRG_NLS_MonoCore_2 | 387 | 392 | PF00514 | 0.627 |
TRG_NLS_MonoExtC_3 | 387 | 393 | PF00514 | 0.623 |
TRG_NLS_MonoExtN_4 | 183 | 188 | PF00514 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I530 | Leptomonas seymouri | 57% | 99% |
A0A1X0P9D0 | Trypanosomatidae | 24% | 100% |
A0A3R7LU18 | Trypanosoma rangeli | 28% | 100% |
A0A3S7X2U8 | Leishmania donovani | 89% | 100% |
A4HHQ1 | Leishmania braziliensis | 79% | 100% |
A4I4W6 | Leishmania infantum | 89% | 100% |
C9ZKZ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AEB4 | Leishmania major | 91% | 100% |
V5C220 | Trypanosoma cruzi | 29% | 100% |