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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 8 |
GO:0005739 | mitochondrion | 5 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A4H9F6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006259 | DNA metabolic process | 4 | 8 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006284 | base-excision repair | 6 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004844 | uracil DNA N-glycosylase activity | 6 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 8 |
GO:0016799 | hydrolase activity, hydrolyzing N-glycosyl compounds | 4 | 8 |
GO:0019104 | DNA N-glycosylase activity | 4 | 8 |
GO:0097506 | deaminated base DNA N-glycosylase activity | 5 | 8 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.622 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.200 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.797 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.200 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.783 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.468 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.674 |
DOC_CYCLIN_yClb1_LxF_4 | 300 | 305 | PF00134 | 0.560 |
DOC_MAPK_gen_1 | 158 | 165 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 173 | 180 | PF00069 | 0.394 |
DOC_PP1_RVXF_1 | 300 | 306 | PF00149 | 0.466 |
DOC_PP2B_LxvP_1 | 368 | 371 | PF13499 | 0.309 |
DOC_PP4_FxxP_1 | 148 | 151 | PF00568 | 0.387 |
DOC_PP4_FxxP_1 | 245 | 248 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.739 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 115 | 120 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 345 | 354 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 356 | 364 | PF00244 | 0.232 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.437 |
LIG_CtBP_PxDLS_1 | 228 | 232 | PF00389 | 0.523 |
LIG_deltaCOP1_diTrp_1 | 144 | 148 | PF00928 | 0.401 |
LIG_deltaCOP1_diTrp_1 | 155 | 162 | PF00928 | 0.408 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.457 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.453 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.446 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.463 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.601 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.508 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.745 |
LIG_LIR_Apic_2 | 147 | 151 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 206 | 214 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 281 | 292 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 144 | 148 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.488 |
LIG_MAD2 | 199 | 207 | PF02301 | 0.464 |
LIG_NRBOX | 302 | 308 | PF00104 | 0.560 |
LIG_PCNA_yPIPBox_3 | 2 | 11 | PF02747 | 0.640 |
LIG_Pex14_2 | 6 | 10 | PF04695 | 0.724 |
LIG_SH2_STAT3 | 311 | 314 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.464 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.396 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.466 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.508 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.668 |
LIG_SUMO_SIM_par_1 | 266 | 271 | PF11976 | 0.464 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.594 |
LIG_TRAF2_2 | 99 | 104 | PF00917 | 0.538 |
LIG_UBA3_1 | 5 | 11 | PF00899 | 0.508 |
LIG_WW_3 | 47 | 51 | PF00397 | 0.509 |
MOD_CDC14_SPxK_1 | 47 | 50 | PF00782 | 0.744 |
MOD_CDK_SPxK_1 | 44 | 50 | PF00069 | 0.756 |
MOD_CDK_SPxxK_3 | 44 | 51 | PF00069 | 0.759 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.760 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.405 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.674 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.490 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.675 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.446 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.474 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.523 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.745 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.721 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.599 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.700 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.309 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.249 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.252 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.505 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.698 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.473 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.506 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.697 |
MOD_LATS_1 | 61 | 67 | PF00433 | 0.539 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.522 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.264 |
MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.532 |
MOD_N-GLC_2 | 191 | 193 | PF02516 | 0.431 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.630 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.464 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.448 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.440 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.663 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.696 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.523 |
MOD_PIKK_1 | 52 | 58 | PF00454 | 0.538 |
MOD_PKA_1 | 62 | 68 | PF00069 | 0.538 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.658 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.290 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.744 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.663 |
MOD_PKB_1 | 28 | 36 | PF00069 | 0.535 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.464 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.530 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.697 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.733 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.464 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.696 |
MOD_SUMO_rev_2 | 104 | 113 | PF00179 | 0.536 |
TRG_DiLeu_BaEn_1 | 258 | 263 | PF01217 | 0.446 |
TRG_DiLeu_BaEn_2 | 143 | 149 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 314 | 319 | PF01217 | 0.388 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 363 | 366 | PF00928 | 0.259 |
TRG_NES_CRM1_1 | 259 | 271 | PF08389 | 0.523 |
TRG_NES_CRM1_1 | 352 | 365 | PF08389 | 0.381 |
TRG_NLS_MonoExtC_3 | 314 | 320 | PF00514 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK50 | Leptomonas seymouri | 54% | 89% |
A0A1X0P6S1 | Trypanosomatidae | 55% | 100% |
A0A3R7L167 | Trypanosoma rangeli | 55% | 100% |
A0A3S7WUW8 | Leishmania donovani | 75% | 95% |
A4HXS3 | Leishmania infantum | 76% | 95% |
E9ARI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
P53766 | Dictyostelium discoideum | 43% | 100% |
Q5UPT2 | Acanthamoeba polyphaga mimivirus | 31% | 100% |
Q8NQU9 | Corynebacterium glutamicum (strain ATCC 13032 / DSM 20300 / BCRC 11384 / JCM 1318 / LMG 3730 / NCIMB 10025) | 38% | 100% |