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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HFM3
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 1 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.235 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.235 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.278 |
CLV_PCSK_PC1ET2_1 | 374 | 376 | PF00082 | 0.258 |
CLV_PCSK_PC7_1 | 74 | 80 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.346 |
DEG_APCC_DBOX_1 | 77 | 85 | PF00400 | 0.476 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.388 |
DOC_CKS1_1 | 7 | 12 | PF01111 | 0.419 |
DOC_CYCLIN_RxL_1 | 90 | 102 | PF00134 | 0.363 |
DOC_CYCLIN_yCln2_LP_2 | 187 | 193 | PF00134 | 0.435 |
DOC_MAPK_gen_1 | 147 | 155 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 78 | 86 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 147 | 155 | PF00069 | 0.515 |
DOC_PP1_RVXF_1 | 283 | 289 | PF00149 | 0.458 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.435 |
DOC_PP4_FxxP_1 | 94 | 97 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.495 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.566 |
LIG_14-3-3_CanoR_1 | 179 | 187 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.480 |
LIG_deltaCOP1_diTrp_1 | 291 | 299 | PF00928 | 0.363 |
LIG_eIF4E_1 | 75 | 81 | PF01652 | 0.476 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.431 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.432 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.510 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.431 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.517 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.363 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.482 |
LIG_LIR_Apic_2 | 93 | 97 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 161 | 169 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 291 | 302 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.454 |
LIG_LRP6_Inhibitor_1 | 98 | 104 | PF00058 | 0.163 |
LIG_PDZ_Class_2 | 374 | 379 | PF00595 | 0.453 |
LIG_SH2_GRB2like | 370 | 373 | PF00017 | 0.453 |
LIG_SH2_STAT3 | 302 | 305 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.435 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 253 | 259 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 150 | 157 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.363 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.432 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.421 |
LIG_TYR_ITIM | 160 | 165 | PF00017 | 0.427 |
LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.453 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.524 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.386 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.437 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.363 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.458 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.297 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.228 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.564 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.436 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.339 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.435 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.515 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.263 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.221 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.235 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.129 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.463 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.463 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.421 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.507 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.421 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.399 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.515 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.500 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.525 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.483 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.475 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.571 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.556 |
TRG_DiLeu_BaEn_1 | 251 | 256 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 76 | 81 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.435 |
TRG_NLS_MonoExtC_3 | 314 | 319 | PF00514 | 0.515 |
TRG_NLS_MonoExtN_4 | 312 | 319 | PF00514 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3Q2 | Leptomonas seymouri | 31% | 100% |
A0A0N1IL51 | Leptomonas seymouri | 66% | 100% |
A0A0S4IY84 | Bodo saltans | 30% | 100% |
A0A0S4JNN8 | Bodo saltans | 45% | 100% |
A0A1X0NWJ2 | Trypanosomatidae | 31% | 100% |
A0A1X0P426 | Trypanosomatidae | 47% | 97% |
A0A3R7K0P4 | Trypanosoma rangeli | 50% | 100% |
A0A3R7LLG2 | Trypanosoma rangeli | 31% | 100% |
A0A3S5H6J9 | Leishmania donovani | 30% | 100% |
A0A3S7X0L2 | Leishmania donovani | 83% | 100% |
A1A4M4 | Bos taurus | 22% | 100% |
A4H6P9 | Leishmania braziliensis | 31% | 87% |
A4HV34 | Leishmania infantum | 30% | 100% |
A4I2Q1 | Leishmania infantum | 83% | 100% |
A4WFX9 | Enterobacter sp. (strain 638) | 27% | 100% |
A7MQN1 | Cronobacter sakazakii (strain ATCC BAA-894) | 28% | 100% |
A8ACY8 | Citrobacter koseri (strain ATCC BAA-895 / CDC 4225-83 / SGSC4696) | 26% | 100% |
A8G8C4 | Serratia proteamaculans (strain 568) | 28% | 100% |
B1JP69 | Yersinia pseudotuberculosis serotype O:3 (strain YPIII) | 26% | 100% |
B2VG45 | Erwinia tasmaniensis (strain DSM 17950 / CFBP 7177 / CIP 109463 / NCPPB 4357 / Et1/99) | 27% | 100% |
B7LTZ5 | Escherichia fergusonii (strain ATCC 35469 / DSM 13698 / CCUG 18766 / IAM 14443 / JCM 21226 / LMG 7866 / NBRC 102419 / NCTC 12128 / CDC 0568-73) | 26% | 100% |
B7XJI2 | Enterocytozoon bieneusi (strain H348) | 23% | 100% |
C6C4V4 | Musicola paradisiaca (strain Ech703) | 25% | 100% |
C6DI71 | Pectobacterium carotovorum subsp. carotovorum (strain PC1) | 25% | 100% |
C9XTA5 | Cronobacter turicensis (strain DSM 18703 / CCUG 55852 / LMG 23827 / z3032) | 28% | 100% |
D0A5V3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 99% |
D0A7B6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0KC77 | Pectobacterium parmentieri (strain WPP163) | 26% | 100% |
D0Z9R0 | Edwardsiella tarda (strain EIB202) | 28% | 100% |
D2TUZ4 | Citrobacter rodentium (strain ICC168) | 26% | 100% |
D4GGR2 | Pantoea ananatis (strain LMG 20103) | 25% | 100% |
D4ICL5 | Erwinia amylovora (strain ATCC 49946 / CCPPB 0273 / Ea273 / 27-3) | 26% | 100% |
D8MKW4 | Erwinia billingiae (strain Eb661) | 27% | 100% |
E0SLH6 | Dickeya dadantii (strain 3937) | 25% | 100% |
E1SKR8 | Pantoea vagans (strain C9-1) | 26% | 100% |
E3G381 | Enterobacter lignolyticus (strain SCF1) | 25% | 100% |
E6WHK1 | Pantoea sp. (strain At-9b) | 26% | 100% |
E8XYF5 | Rahnella sp. (strain Y9602) | 27% | 100% |
E9AD77 | Leishmania major | 83% | 100% |
E9ANR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AZ01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
P27859 | Escherichia coli (strain K12) | 25% | 100% |
P34220 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 91% |
P37545 | Bacillus subtilis (strain 168) | 22% | 100% |
P57436 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 21% | 100% |
Q0SZ31 | Shigella flexneri serotype 5b (strain 8401) | 25% | 100% |
Q148G4 | Bos taurus | 31% | 100% |
Q17R31 | Homo sapiens | 22% | 100% |
Q4QGV4 | Leishmania major | 30% | 100% |
Q640V9 | Xenopus laevis | 33% | 100% |
Q6DAQ1 | Pectobacterium atrosepticum (strain SCRI 1043 / ATCC BAA-672) | 25% | 100% |
Q6GML7 | Danio rerio | 31% | 100% |
Q6P1N9 | Homo sapiens | 31% | 100% |
Q6P8M1 | Mus musculus | 32% | 100% |
Q89AG7 | Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) | 20% | 100% |
Q8SW70 | Encephalitozoon cuniculi (strain GB-M1) | 25% | 100% |
Q9L6M2 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 27% | 100% |
Q9UUF1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
V5BRW2 | Trypanosoma cruzi | 30% | 100% |