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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HMW6
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004518 | nuclease activity | 4 | 12 |
GO:0004527 | exonuclease activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008270 | zinc ion binding | 6 | 12 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0046914 | transition metal ion binding | 5 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.276 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.527 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.256 |
CLV_PCSK_PC7_1 | 205 | 211 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.200 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.736 |
DEG_SCF_FBW7_1 | 20 | 26 | PF00400 | 0.617 |
DOC_ANK_TNKS_1 | 317 | 324 | PF00023 | 0.404 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.700 |
DOC_CYCLIN_RxL_1 | 163 | 171 | PF00134 | 0.490 |
DOC_CYCLIN_yCln2_LP_2 | 79 | 85 | PF00134 | 0.403 |
DOC_MAPK_gen_1 | 101 | 109 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 188 | 195 | PF00069 | 0.581 |
DOC_MAPK_gen_1 | 90 | 98 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 101 | 109 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 188 | 197 | PF00069 | 0.492 |
DOC_MAPK_NFAT4_5 | 188 | 196 | PF00069 | 0.581 |
DOC_PP1_RVXF_1 | 164 | 171 | PF00149 | 0.487 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.529 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 125 | 129 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 210 | 216 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 25 | 33 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 285 | 291 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 348 | 352 | PF00244 | 0.554 |
LIG_BIR_III_2 | 305 | 309 | PF00653 | 0.484 |
LIG_BRCT_BRCA1_1 | 267 | 271 | PF00533 | 0.504 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.675 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.538 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.459 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.517 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.345 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.516 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.538 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.524 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.558 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.442 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.581 |
LIG_LIR_Apic_2 | 317 | 322 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 56 | 66 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 10 | 15 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 268 | 274 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.732 |
LIG_MLH1_MIPbox_1 | 267 | 271 | PF16413 | 0.504 |
LIG_Pex14_1 | 315 | 319 | PF04695 | 0.395 |
LIG_Rb_pABgroove_1 | 136 | 144 | PF01858 | 0.487 |
LIG_REV1ctd_RIR_1 | 167 | 178 | PF16727 | 0.537 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.537 |
LIG_SH2_PTP2 | 319 | 322 | PF00017 | 0.411 |
LIG_SH2_STAT3 | 81 | 84 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.391 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.608 |
LIG_SUMO_SIM_par_1 | 143 | 148 | PF11976 | 0.477 |
LIG_WRC_WIRS_1 | 325 | 330 | PF05994 | 0.558 |
MOD_CDK_SPxK_1 | 19 | 25 | PF00069 | 0.720 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.503 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.501 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.706 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.536 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.458 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.475 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.444 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.538 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.666 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.287 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.704 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.568 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.557 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.635 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.400 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.616 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.613 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.535 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.464 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.659 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.655 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.738 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.550 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.405 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.616 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.517 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.528 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.504 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.540 |
MOD_NEK2_1 | 378 | 383 | PF00069 | 0.473 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.530 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.400 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.516 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.757 |
MOD_PIKK_1 | 272 | 278 | PF00454 | 0.541 |
MOD_PK_1 | 203 | 209 | PF00069 | 0.487 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.501 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.476 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.389 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.553 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.581 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.537 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.400 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.501 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.588 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.565 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.693 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.504 |
MOD_SUMO_rev_2 | 87 | 95 | PF00179 | 0.581 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 166 | 171 | PF00026 | 0.271 |
TRG_Pf-PMV_PEXEL_1 | 189 | 194 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.756 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.200 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWS9 | Leptomonas seymouri | 79% | 97% |
A0A0S4JGY9 | Bodo saltans | 50% | 100% |
A0A1X0P5F6 | Trypanosomatidae | 67% | 100% |
A0A3R7KR79 | Trypanosoma rangeli | 67% | 100% |
A0A3S7X9G9 | Leishmania donovani | 88% | 100% |
A4IBI7 | Leishmania infantum | 88% | 100% |
C9ZZ53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
E9AFC3 | Leishmania major | 88% | 100% |
E9B6H8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5BY58 | Trypanosoma cruzi | 67% | 100% |