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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B358
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004518 | nuclease activity | 4 | 6 |
GO:0004527 | exonuclease activity | 5 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.695 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.695 |
DEG_SIAH_1 | 49 | 57 | PF03145 | 0.620 |
DOC_PP2B_LxvP_1 | 68 | 71 | PF13499 | 0.688 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.442 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.590 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.791 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.588 |
LIG_14-3-3_CanoR_1 | 185 | 194 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 31 | 37 | PF00244 | 0.689 |
LIG_14-3-3_CterR_2 | 342 | 347 | PF00244 | 0.411 |
LIG_Actin_WH2_2 | 120 | 135 | PF00022 | 0.590 |
LIG_Actin_WH2_2 | 59 | 75 | PF00022 | 0.592 |
LIG_BIR_III_2 | 14 | 18 | PF00653 | 0.663 |
LIG_BRCT_BRCA1_1 | 101 | 105 | PF00533 | 0.463 |
LIG_deltaCOP1_diTrp_1 | 165 | 175 | PF00928 | 0.540 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.649 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.590 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.715 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.458 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.540 |
LIG_GBD_Chelix_1 | 211 | 219 | PF00786 | 0.339 |
LIG_LIR_Gen_1 | 102 | 112 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 198 | 207 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 284 | 295 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 198 | 202 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.659 |
LIG_LYPXL_yS_3 | 292 | 295 | PF13949 | 0.540 |
LIG_NRBOX | 326 | 332 | PF00104 | 0.590 |
LIG_Pex14_1 | 275 | 279 | PF04695 | 0.540 |
LIG_Pex14_1 | 339 | 343 | PF04695 | 0.614 |
LIG_Pex14_2 | 257 | 261 | PF04695 | 0.482 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.590 |
LIG_SH2_PTP2 | 178 | 181 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.540 |
LIG_SH2_STAT6 | 270 | 274 | PF00017 | 0.590 |
LIG_SH3_1 | 178 | 184 | PF00018 | 0.540 |
LIG_SH3_2 | 181 | 186 | PF14604 | 0.590 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.590 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.506 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.500 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.578 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.472 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.738 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.774 |
LIG_SUMO_SIM_par_1 | 108 | 115 | PF11976 | 0.540 |
LIG_TRAF2_2 | 9 | 14 | PF00917 | 0.646 |
LIG_TYR_ITIM | 216 | 221 | PF00017 | 0.590 |
LIG_TYR_ITIM | 290 | 295 | PF00017 | 0.590 |
MOD_CDK_SPK_2 | 26 | 31 | PF00069 | 0.647 |
MOD_CDK_SPK_2 | 52 | 57 | PF00069 | 0.619 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.585 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.750 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.775 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.747 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.540 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.478 |
MOD_Cter_Amidation | 4 | 7 | PF01082 | 0.655 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.465 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.312 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.312 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.582 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.279 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.747 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.697 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.506 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.585 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.479 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.700 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.687 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.695 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.517 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.559 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.312 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.482 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.526 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.641 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.505 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.659 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.603 |
MOD_OFUCOSY | 100 | 107 | PF10250 | 0.541 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.714 |
MOD_PKA_1 | 185 | 191 | PF00069 | 0.544 |
MOD_PKA_1 | 337 | 343 | PF00069 | 0.335 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.506 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.618 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.527 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.478 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.478 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.569 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.584 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.680 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.478 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.690 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.664 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.697 |
TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.630 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBJ5 | Leptomonas seymouri | 44% | 85% |
A4HKS0 | Leishmania braziliensis | 78% | 100% |
D0AAH2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 95% |
V5BHY6 | Trypanosoma cruzi | 34% | 100% |