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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HK12
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 7 |
GO:0016799 | hydrolase activity, hydrolyzing N-glycosyl compounds | 4 | 7 |
GO:0019104 | DNA N-glycosylase activity | 4 | 7 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 7 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.605 |
CLV_PCSK_FUR_1 | 175 | 179 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.576 |
CLV_PCSK_PC7_1 | 174 | 180 | PF00082 | 0.473 |
CLV_PCSK_PC7_1 | 26 | 32 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.549 |
DOC_CKS1_1 | 202 | 207 | PF01111 | 0.332 |
DOC_CYCLIN_RxL_1 | 110 | 121 | PF00134 | 0.308 |
DOC_CYCLIN_RxL_1 | 279 | 293 | PF00134 | 0.504 |
DOC_MAPK_FxFP_2 | 102 | 105 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 299 | 306 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 299 | 308 | PF00069 | 0.349 |
DOC_PP1_RVXF_1 | 155 | 162 | PF00149 | 0.571 |
DOC_PP1_RVXF_1 | 258 | 264 | PF00149 | 0.365 |
DOC_PP1_RVXF_1 | 96 | 103 | PF00149 | 0.493 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.513 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.629 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.537 |
LIG_14-3-3_CanoR_1 | 179 | 188 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 26 | 33 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 279 | 289 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 8 | 12 | PF00244 | 0.645 |
LIG_BRCT_BRCA1_1 | 98 | 102 | PF00533 | 0.588 |
LIG_Clathr_ClatBox_1 | 117 | 121 | PF01394 | 0.326 |
LIG_deltaCOP1_diTrp_1 | 110 | 119 | PF00928 | 0.432 |
LIG_eIF4E_1 | 6 | 12 | PF01652 | 0.450 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.605 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.620 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.500 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.431 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.663 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.647 |
LIG_FHA_2 | 231 | 237 | PF00498 | 0.641 |
LIG_LIR_Apic_2 | 99 | 105 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.202 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.460 |
LIG_MAD2 | 86 | 94 | PF02301 | 0.545 |
LIG_NRBOX | 217 | 223 | PF00104 | 0.443 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.537 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.445 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.439 |
LIG_SH2_NCK_1 | 127 | 131 | PF00017 | 0.496 |
LIG_SH2_NCK_1 | 252 | 256 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.597 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.495 |
LIG_SUMO_SIM_anti_2 | 7 | 13 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 213 | 219 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.397 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.394 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.641 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.483 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.536 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.436 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.515 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.453 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.635 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.397 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.526 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.606 |
MOD_GlcNHglycan | 223 | 228 | PF01048 | 0.482 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.455 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.657 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.527 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.730 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.454 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.437 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.600 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.447 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.485 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.617 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.536 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.454 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.568 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.495 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.539 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.380 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.397 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.464 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.412 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.369 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.549 |
MOD_PK_1 | 66 | 72 | PF00069 | 0.461 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.407 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.518 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.463 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.565 |
MOD_PKB_1 | 177 | 185 | PF00069 | 0.516 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.442 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.568 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.461 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.544 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.462 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.536 |
MOD_SUMO_rev_2 | 290 | 295 | PF00179 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 132 | 137 | PF01217 | 0.479 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAV6 | Leptomonas seymouri | 56% | 100% |
A0A3S7X534 | Leishmania donovani | 80% | 100% |
A4I7J6 | Leishmania infantum | 81% | 100% |
E9B2F3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q5Q3 | Leishmania major | 81% | 100% |