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 | 2 |
GO:0005930 | axoneme | 2 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AFR6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004427 | inorganic diphosphate phosphatase activity | 6 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.586 |
CLV_PCSK_PC7_1 | 309 | 315 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.399 |
DEG_SCF_FBW7_1 | 6 | 12 | PF00400 | 0.509 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.508 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.539 |
DOC_CYCLIN_yCln2_LP_2 | 132 | 138 | PF00134 | 0.322 |
DOC_MAPK_gen_1 | 123 | 132 | PF00069 | 0.484 |
DOC_MAPK_gen_1 | 262 | 270 | PF00069 | 0.438 |
DOC_MAPK_HePTP_8 | 162 | 174 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 112 | 120 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 165 | 174 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 262 | 270 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 324 | 333 | PF00069 | 0.339 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.477 |
DOC_PP4_FxxP_1 | 356 | 359 | PF00568 | 0.526 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.504 |
DOC_USP7_UBL2_3 | 143 | 147 | PF12436 | 0.498 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.523 |
LIG_14-3-3_CanoR_1 | 201 | 205 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.327 |
LIG_14-3-3_CanoR_1 | 271 | 277 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 314 | 323 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 350 | 359 | PF00244 | 0.441 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.620 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.436 |
LIG_deltaCOP1_diTrp_1 | 368 | 374 | PF00928 | 0.385 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.400 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.321 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.505 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.652 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.639 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.547 |
LIG_LIR_Apic_2 | 122 | 127 | PF02991 | 0.479 |
LIG_LIR_Apic_2 | 353 | 359 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 246 | 257 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.352 |
LIG_LYPXL_yS_3 | 3 | 6 | PF13949 | 0.480 |
LIG_Pex14_1 | 370 | 374 | PF04695 | 0.380 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.329 |
LIG_SH2_GRB2like | 378 | 381 | PF00017 | 0.524 |
LIG_SH2_PTP2 | 161 | 164 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.251 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 57 | 65 | PF11976 | 0.532 |
LIG_TRAF2_1 | 277 | 280 | PF00917 | 0.591 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.469 |
LIG_TYR_ITIM | 247 | 252 | PF00017 | 0.415 |
LIG_WRC_WIRS_1 | 216 | 221 | PF05994 | 0.335 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.456 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.488 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.591 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.480 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.454 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.601 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.464 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.521 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.509 |
MOD_GlcNHglycan | 390 | 394 | PF01048 | 0.577 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.475 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.686 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.339 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.444 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.489 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.596 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.708 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.577 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.485 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.572 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.332 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.471 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.416 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.552 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.417 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.424 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.546 |
MOD_PKB_1 | 80 | 88 | PF00069 | 0.531 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.440 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.599 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.527 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.620 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.436 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.324 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.590 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.658 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.532 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.377 |
TRG_DiLeu_BaEn_1 | 97 | 102 | PF01217 | 0.414 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.558 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 99 | 104 | PF00026 | 0.422 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P968 | Leptomonas seymouri | 75% | 100% |
A0A0S4JSR6 | Bodo saltans | 45% | 70% |
A0A1X0P6F9 | Trypanosomatidae | 57% | 100% |
A0A3R7KSW5 | Trypanosoma rangeli | 54% | 100% |
A0A3S7X9V3 | Leishmania donovani | 94% | 100% |
A4HNA8 | Leishmania braziliensis | 80% | 100% |
A4IBX9 | Leishmania infantum | 94% | 100% |
C9ZYM8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9B6W9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q9H0C1 | Homo sapiens | 27% | 100% |
V5BXU3 | Trypanosoma cruzi | 54% | 100% |