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. | yes | yes: 10 |
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: 2 |
NetGPI | no | yes: 0, no: 2 |
Related structures:
AlphaFold database: A4HL71
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 3 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0005515 | protein binding | 2 | 3 |
GO:0005524 | ATP binding | 5 | 3 |
GO:0016462 | pyrophosphatase activity | 5 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 3 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 3 |
GO:0016887 | ATP hydrolysis activity | 7 | 3 |
GO:0017076 | purine nucleotide binding | 4 | 3 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 3 |
GO:0030554 | adenyl nucleotide binding | 5 | 3 |
GO:0032553 | ribonucleotide binding | 3 | 3 |
GO:0032555 | purine ribonucleotide binding | 4 | 3 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 3 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 3 |
GO:0036094 | small molecule binding | 2 | 3 |
GO:0043167 | ion binding | 2 | 3 |
GO:0043168 | anion binding | 3 | 3 |
GO:0044183 | protein folding chaperone | 1 | 3 |
GO:0051082 | unfolded protein binding | 3 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:0097367 | carbohydrate derivative binding | 2 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 3 |
GO:1901265 | nucleoside phosphate binding | 3 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.539 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 340 | 344 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.539 |
CLV_Separin_Metazoa | 111 | 115 | PF03568 | 0.539 |
DEG_APCC_DBOX_1 | 105 | 113 | PF00400 | 0.539 |
DEG_APCC_DBOX_1 | 162 | 170 | PF00400 | 0.526 |
DEG_Kelch_Keap1_1 | 117 | 122 | PF01344 | 0.539 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.252 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.842 |
DOC_CYCLIN_RxL_1 | 63 | 76 | PF00134 | 0.270 |
DOC_MAPK_gen_1 | 106 | 115 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 160 | 170 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 307 | 317 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 337 | 346 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 6 | 15 | PF00069 | 0.530 |
DOC_MAPK_HePTP_8 | 238 | 250 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 162 | 170 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 241 | 250 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 310 | 317 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 337 | 346 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.530 |
DOC_MAPK_NFAT4_5 | 8 | 16 | PF00069 | 0.530 |
DOC_PP1_RVXF_1 | 308 | 315 | PF00149 | 0.539 |
DOC_PP2B_PxIxI_1 | 245 | 251 | PF00149 | 0.539 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.842 |
DOC_USP7_UBL2_3 | 135 | 139 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 60 | 64 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.539 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 114 | 124 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 241 | 246 | PF00244 | 0.539 |
LIG_Actin_WH2_2 | 256 | 272 | PF00022 | 0.539 |
LIG_APCC_ABBA_1 | 71 | 76 | PF00400 | 0.539 |
LIG_APCC_ABBA_1 | 97 | 102 | PF00400 | 0.539 |
LIG_APCC_ABBAyCdc20_2 | 196 | 202 | PF00400 | 0.539 |
LIG_APCC_ABBAyCdc20_2 | 96 | 102 | PF00400 | 0.539 |
LIG_BRCT_BRCA1_1 | 153 | 157 | PF00533 | 0.402 |
LIG_deltaCOP1_diTrp_1 | 30 | 34 | PF00928 | 0.539 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.539 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.539 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.539 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.539 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.539 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.325 |
LIG_IRF3_LxIS_1 | 44 | 49 | PF10401 | 0.539 |
LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 311 | 322 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 72 | 78 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 30 | 34 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 311 | 317 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 82 | 87 | PF02991 | 0.387 |
LIG_NRBOX | 108 | 114 | PF00104 | 0.539 |
LIG_NRBOX | 311 | 317 | PF00104 | 0.539 |
LIG_PCNA_yPIPBox_3 | 50 | 62 | PF02747 | 0.539 |
LIG_Pex14_2 | 87 | 91 | PF04695 | 0.539 |
LIG_Rb_pABgroove_1 | 311 | 319 | PF01858 | 0.539 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.539 |
LIG_SH2_STAT3 | 178 | 181 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.539 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.539 |
LIG_SH3_4 | 135 | 142 | PF00018 | 0.270 |
LIG_TRAF2_1 | 120 | 123 | PF00917 | 0.539 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.539 |
LIG_UBA3_1 | 58 | 64 | PF00899 | 0.539 |
LIG_UBA3_1 | 73 | 81 | PF00899 | 0.292 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.539 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.539 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.539 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.539 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.539 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.210 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.325 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.534 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.760 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.539 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.539 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.539 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.539 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.539 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.790 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.539 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.539 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.539 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.292 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.539 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.539 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.539 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.539 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.539 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.539 |
MOD_Plk_2-3 | 123 | 129 | PF00069 | 0.539 |
MOD_Plk_2-3 | 234 | 240 | PF00069 | 0.402 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.539 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.539 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.539 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.539 |
MOD_SUMO_for_1 | 134 | 137 | PF00179 | 0.402 |
MOD_SUMO_rev_2 | 185 | 192 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 206 | 216 | PF00179 | 0.525 |
MOD_SUMO_rev_2 | 79 | 87 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_2 | 152 | 158 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_4 | 122 | 128 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.473 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.539 |
TRG_NES_CRM1_1 | 227 | 240 | PF08389 | 0.539 |
TRG_NES_CRM1_1 | 336 | 352 | PF08389 | 0.539 |
TRG_NLS_MonoExtC_3 | 105 | 111 | PF00514 | 0.539 |
TRG_NLS_MonoExtN_4 | 4 | 10 | PF00514 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.539 |