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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q5I1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 4 |
GO:0016791 | phosphatase activity | 5 | 4 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.563 |
CLV_C14_Caspase3-7 | 380 | 384 | PF00656 | 0.479 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.275 |
CLV_PCSK_PC1ET2_1 | 60 | 62 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.256 |
DEG_SPOP_SBC_1 | 275 | 279 | PF00917 | 0.635 |
DOC_CYCLIN_RxL_1 | 106 | 117 | PF00134 | 0.478 |
DOC_CYCLIN_RxL_1 | 57 | 66 | PF00134 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 15 | PF00134 | 0.475 |
DOC_MAPK_gen_1 | 118 | 125 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 164 | 174 | PF00069 | 0.529 |
DOC_MAPK_MEF2A_6 | 167 | 174 | PF00069 | 0.529 |
DOC_MAPK_NFAT4_5 | 167 | 175 | PF00069 | 0.529 |
DOC_PP1_RVXF_1 | 108 | 115 | PF00149 | 0.475 |
DOC_PP2B_LxvP_1 | 11 | 14 | PF13499 | 0.315 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.488 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.475 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.472 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 223 | 230 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 276 | 281 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 409 | 413 | PF00244 | 0.637 |
LIG_APCC_ABBA_1 | 170 | 175 | PF00400 | 0.529 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.751 |
LIG_CaM_IQ_9 | 186 | 201 | PF13499 | 0.399 |
LIG_Clathr_ClatBox_1 | 171 | 175 | PF01394 | 0.529 |
LIG_Clathr_ClatBox_1 | 49 | 53 | PF01394 | 0.475 |
LIG_deltaCOP1_diTrp_1 | 117 | 125 | PF00928 | 0.475 |
LIG_EVH1_2 | 14 | 18 | PF00568 | 0.475 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.579 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.485 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.529 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.553 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.635 |
LIG_LIR_Apic_2 | 371 | 375 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 157 | 166 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 16 | 26 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 269 | 275 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.558 |
LIG_MYND_1 | 10 | 14 | PF01753 | 0.312 |
LIG_Pex14_1 | 353 | 357 | PF04695 | 0.368 |
LIG_Pex14_2 | 173 | 177 | PF04695 | 0.529 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.529 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.551 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.452 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.475 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.743 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.621 |
LIG_SUMO_SIM_anti_2 | 45 | 51 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 240 | 248 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.478 |
LIG_TRAF2_1 | 31 | 34 | PF00917 | 0.478 |
LIG_TRAF2_1 | 363 | 366 | PF00917 | 0.409 |
LIG_TYR_ITIM | 395 | 400 | PF00017 | 0.430 |
MOD_CDK_SPK_2 | 101 | 106 | PF00069 | 0.443 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.488 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.681 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.595 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.540 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.569 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.559 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.475 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.486 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.651 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.636 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.693 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.568 |
MOD_CMANNOS | 353 | 356 | PF00535 | 0.373 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.297 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.411 |
MOD_GlcNHglycan | 231 | 235 | PF01048 | 0.592 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.706 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.283 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.599 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.639 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.546 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.291 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.603 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.496 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.659 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.483 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.653 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.717 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.523 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.529 |
MOD_LATS_1 | 219 | 225 | PF00433 | 0.476 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.286 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.585 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.522 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.461 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.725 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.653 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.540 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.570 |
MOD_PKA_1 | 327 | 333 | PF00069 | 0.559 |
MOD_PKA_2 | 166 | 172 | PF00069 | 0.496 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.643 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.630 |
MOD_PKA_2 | 408 | 414 | PF00069 | 0.641 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.460 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.601 |
MOD_Plk_2-3 | 222 | 228 | PF00069 | 0.522 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.588 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.705 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.570 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.587 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.496 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.488 |
MOD_SUMO_rev_2 | 339 | 349 | PF00179 | 0.561 |
MOD_SUMO_rev_2 | 365 | 369 | PF00179 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 58 | 63 | PF01217 | 0.529 |
TRG_DiLeu_BaLyEn_6 | 7 | 12 | PF01217 | 0.522 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 141 | 143 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.502 |
TRG_NLS_Bipartite_1 | 194 | 213 | PF00514 | 0.466 |
TRG_NLS_MonoExtN_4 | 208 | 213 | PF00514 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 61 | 66 | PF00026 | 0.303 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE45 | Leptomonas seymouri | 59% | 99% |
A0A3Q8IT66 | Leishmania donovani | 92% | 100% |
A4HK83 | Leishmania braziliensis | 76% | 100% |
A4I7R8 | Leishmania infantum | 93% | 100% |
E9B2M6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |