Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 1 |
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. | yes | yes: 15 |
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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A4HIH9
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0044183 | protein folding chaperone | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.480 |
CLV_PCSK_FUR_1 | 251 | 255 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 253 | 255 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.464 |
DEG_APCC_KENBOX_2 | 284 | 288 | PF00400 | 0.480 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.223 |
DOC_MAPK_gen_1 | 219 | 225 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 191 | 200 | PF00069 | 0.357 |
DOC_MAPK_RevD_3 | 131 | 146 | PF00069 | 0.239 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.705 |
DOC_USP7_UBL2_3 | 285 | 289 | PF12436 | 0.493 |
DOC_USP7_UBL2_3 | 45 | 49 | PF12436 | 0.472 |
DOC_WW_Pin1_4 | 116 | 121 | PF00397 | 0.384 |
LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.287 |
LIG_BIR_III_4 | 203 | 207 | PF00653 | 0.464 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.359 |
LIG_Clathr_ClatBox_1 | 113 | 117 | PF01394 | 0.384 |
LIG_CtBP_PxDLS_1 | 120 | 124 | PF00389 | 0.380 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.420 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.453 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.480 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.484 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.360 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.463 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.403 |
LIG_LIR_Gen_1 | 147 | 155 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 276 | 280 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 84 | 89 | PF02991 | 0.495 |
LIG_REV1ctd_RIR_1 | 78 | 84 | PF16727 | 0.384 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.481 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.287 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.390 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.464 |
LIG_SUMO_SIM_anti_2 | 60 | 65 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 112 | 117 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 119 | 126 | PF11976 | 0.365 |
LIG_SxIP_EBH_1 | 135 | 146 | PF03271 | 0.421 |
LIG_UBA3_1 | 131 | 138 | PF00899 | 0.231 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.387 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.693 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.231 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.532 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.432 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.331 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.386 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.736 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.590 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.483 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.350 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.430 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.396 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.667 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.278 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.451 |
MOD_PIKK_1 | 262 | 268 | PF00454 | 0.472 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.416 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.522 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.304 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.237 |
MOD_ProDKin_1 | 116 | 122 | PF00069 | 0.384 |
MOD_SUMO_for_1 | 160 | 163 | PF00179 | 0.231 |
MOD_SUMO_for_1 | 252 | 255 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 271 | 280 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 50 | 58 | PF00179 | 0.380 |
MOD_SUMO_rev_2 | 75 | 80 | PF00179 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 32 | 37 | PF01217 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.222 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NYN5 | Trypanosomatidae | 42% | 91% |
A4HIH7 | Leishmania braziliensis | 99% | 100% |
C9ZRV1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 69% |
E9B0A0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
V5B942 | Trypanosoma cruzi | 41% | 77% |
V5BZ53 | Trypanosoma cruzi | 41% | 74% |