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: 0 |
Pissara et al. | no | yes: 3 |
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: 34 |
NetGPI | no | yes: 0, no: 34 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8IAY1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 33 |
GO:0016787 | hydrolase activity | 2 | 33 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.311 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.279 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.387 |
DOC_MAPK_gen_1 | 252 | 260 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 319 | 326 | PF00069 | 0.427 |
DOC_PP1_RVXF_1 | 234 | 240 | PF00149 | 0.389 |
DOC_PP1_RVXF_1 | 348 | 355 | PF00149 | 0.350 |
DOC_PP4_FxxP_1 | 48 | 51 | PF00568 | 0.344 |
DOC_PP4_FxxP_1 | 76 | 79 | PF00568 | 0.344 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.343 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.340 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.240 |
LIG_14-3-3_CanoR_1 | 169 | 176 | PF00244 | 0.153 |
LIG_14-3-3_CanoR_1 | 212 | 216 | PF00244 | 0.184 |
LIG_14-3-3_CanoR_1 | 294 | 300 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 305 | 311 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.421 |
LIG_BIR_III_4 | 160 | 164 | PF00653 | 0.388 |
LIG_BRCT_BRCA1_1 | 44 | 48 | PF00533 | 0.315 |
LIG_EVH1_1 | 48 | 52 | PF00568 | 0.339 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.247 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.333 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.293 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.175 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.425 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.390 |
LIG_HP1_1 | 322 | 326 | PF01393 | 0.389 |
LIG_HP1_1 | 332 | 336 | PF01393 | 0.389 |
LIG_IRF3_LxIS_1 | 164 | 171 | PF10401 | 0.300 |
LIG_LIR_Apic_2 | 127 | 132 | PF02991 | 0.390 |
LIG_LIR_Apic_2 | 45 | 51 | PF02991 | 0.534 |
LIG_LIR_Apic_2 | 74 | 79 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.191 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 6 | 14 | PF02991 | 0.454 |
LIG_LIR_LC3C_4 | 331 | 335 | PF02991 | 0.184 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.323 |
LIG_Pex14_1 | 97 | 101 | PF04695 | 0.245 |
LIG_REV1ctd_RIR_1 | 237 | 245 | PF16727 | 0.201 |
LIG_SH2_CRK | 366 | 370 | PF00017 | 0.225 |
LIG_SH2_GRB2like | 115 | 118 | PF00017 | 0.294 |
LIG_SH2_PTP2 | 9 | 12 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.460 |
LIG_SH3_1 | 46 | 52 | PF00018 | 0.332 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.364 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.677 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.312 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.540 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.416 |
LIG_SUMO_SIM_anti_2 | 331 | 337 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 331 | 337 | PF11976 | 0.184 |
MOD_CDK_SPxK_1 | 313 | 319 | PF00069 | 0.153 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.664 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.265 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.327 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.325 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.402 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.449 |
MOD_Cter_Amidation | 270 | 273 | PF01082 | 0.201 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.373 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.322 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.400 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.216 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.735 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.331 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.724 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.426 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.377 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.183 |
MOD_N-GLC_1 | 90 | 95 | PF02516 | 0.201 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.310 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.289 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.273 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.244 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.235 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.383 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.387 |
MOD_NEK2_2 | 245 | 250 | PF00069 | 0.350 |
MOD_PIKK_1 | 168 | 174 | PF00454 | 0.201 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.294 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.387 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.446 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.423 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.153 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.542 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.450 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.415 |
MOD_Plk_2-3 | 228 | 234 | PF00069 | 0.389 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.353 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.379 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.400 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.340 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.635 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.240 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.460 |
TRG_ER_diArg_1 | 235 | 238 | PF00400 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3D3 | Leptomonas seymouri | 37% | 90% |
A0A0N0P3S4 | Leptomonas seymouri | 62% | 100% |
A0A0N1PA10 | Leptomonas seymouri | 37% | 100% |
A0A0N1PCQ2 | Leptomonas seymouri | 43% | 100% |
A0A0S4JQB3 | Bodo saltans | 36% | 100% |
A0A1X0NSR3 | Trypanosomatidae | 35% | 87% |
A0A1X0NSS6 | Trypanosomatidae | 41% | 100% |
A0A3R7KKJ0 | Trypanosoma rangeli | 39% | 100% |
A0A3S5IRR1 | Trypanosoma rangeli | 33% | 96% |
A0A3S7WUJ3 | Leishmania donovani | 40% | 100% |
A0A3S7WUK0 | Leishmania donovani | 38% | 90% |
A0A3S7X1K2 | Leishmania donovani | 36% | 100% |
A0A422NS41 | Trypanosoma rangeli | 35% | 91% |
A4H956 | Leishmania braziliensis | 41% | 100% |
A4H959 | Leishmania braziliensis | 36% | 100% |
A4H960 | Leishmania braziliensis | 76% | 100% |
A4HGL0 | Leishmania braziliensis | 38% | 100% |
A4HXH8 | Leishmania infantum | 40% | 100% |
A4HXI1 | Leishmania infantum | 38% | 100% |
A4HXI2 | Leishmania infantum | 100% | 100% |
A4I3N6 | Leishmania infantum | 36% | 100% |
C9ZP70 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AR73 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 98% |
E9AR76 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AR77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AZX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
Q4Q8A8 | Leishmania major | 36% | 100% |
Q4QE86 | Leishmania major | 94% | 100% |
Q4QE87 | Leishmania major | 37% | 100% |
Q4QE90 | Leishmania major | 40% | 100% |
Q54528 | Streptomyces purpurascens | 27% | 100% |
Q54809 | Streptomyces peucetius | 27% | 100% |
Q55217 | Streptomyces sp. (strain C5) | 28% | 100% |
V5AZB9 | Trypanosoma cruzi | 34% | 91% |
V5BER0 | Trypanosoma cruzi | 40% | 100% |
V5BNU9 | Trypanosoma cruzi | 31% | 96% |