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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q851
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006284 | base-excision repair | 6 | 12 |
GO:0006298 | mismatch repair | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000700 | mismatch base pair DNA N-glycosylase activity | 5 | 12 |
GO:0000701 | purine-specific mismatch base pair DNA N-glycosylase activity | 6 | 12 |
GO:0000702 | oxidized base lesion DNA N-glycosylase activity | 5 | 2 |
GO:0003676 | nucleic acid binding | 3 | 5 |
GO:0003677 | DNA binding | 4 | 5 |
GO:0003684 | damaged DNA binding | 5 | 2 |
GO:0003690 | double-stranded DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008534 | oxidized purine nucleobase lesion DNA N-glycosylase activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 12 |
GO:0016799 | hydrolase activity, hydrolyzing N-glycosyl compounds | 4 | 12 |
GO:0019104 | DNA N-glycosylase activity | 4 | 12 |
GO:0030983 | mismatched DNA binding | 6 | 2 |
GO:0032356 | oxidized DNA binding | 6 | 2 |
GO:0032357 | oxidized purine DNA binding | 7 | 2 |
GO:0034039 | 8-oxo-7,8-dihydroguanine DNA N-glycosylase activity | 7 | 2 |
GO:0035485 | adenine/guanine mispair binding | 7 | 2 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0051536 | iron-sulfur cluster binding | 3 | 12 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 12 |
GO:0051540 | metal cluster binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
GO:0004518 | nuclease activity | 4 | 2 |
GO:0004519 | endonuclease activity | 5 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 482 | 486 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.325 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.313 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 107 | 109 | PF00082 | 0.231 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 414 | 416 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 477 | 479 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.296 |
DEG_APCC_DBOX_1 | 452 | 460 | PF00400 | 0.427 |
DEG_SCF_FBW7_1 | 16 | 21 | PF00400 | 0.660 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.634 |
DOC_CYCLIN_yCln2_LP_2 | 361 | 367 | PF00134 | 0.372 |
DOC_MAPK_gen_1 | 303 | 311 | PF00069 | 0.425 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.537 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.500 |
DOC_SPAK_OSR1_1 | 325 | 329 | PF12202 | 0.338 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 457 | 461 | PF12436 | 0.389 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.732 |
LIG_14-3-3_CanoR_1 | 386 | 396 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 70 | 80 | PF00244 | 0.580 |
LIG_Actin_WH2_2 | 191 | 208 | PF00022 | 0.389 |
LIG_BIR_III_4 | 406 | 410 | PF00653 | 0.372 |
LIG_BRCT_BRCA1_1 | 183 | 187 | PF00533 | 0.451 |
LIG_BRCT_BRCA1_2 | 183 | 189 | PF00533 | 0.389 |
LIG_deltaCOP1_diTrp_1 | 14 | 22 | PF00928 | 0.589 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.389 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.591 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.556 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.466 |
LIG_LIR_Apic_2 | 14 | 18 | PF02991 | 0.638 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 377 | 385 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 342 | 346 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 377 | 381 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.520 |
LIG_LRP6_Inhibitor_1 | 194 | 200 | PF00058 | 0.337 |
LIG_PCNA_yPIPBox_3 | 29 | 39 | PF02747 | 0.428 |
LIG_PCNA_yPIPBox_3 | 330 | 341 | PF02747 | 0.372 |
LIG_Pex14_1 | 105 | 109 | PF04695 | 0.451 |
LIG_RPA_C_Fungi | 319 | 331 | PF08784 | 0.411 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.417 |
LIG_SH2_NCK_1 | 177 | 181 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 177 | 181 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.294 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.295 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.315 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.380 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.360 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.410 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.423 |
LIG_TRAF2_1 | 30 | 33 | PF00917 | 0.506 |
LIG_TRAF2_1 | 479 | 482 | PF00917 | 0.726 |
LIG_UBA3_1 | 455 | 461 | PF00899 | 0.431 |
LIG_WRC_WIRS_1 | 19 | 24 | PF05994 | 0.573 |
MOD_CDC14_SPxK_1 | 488 | 491 | PF00782 | 0.758 |
MOD_CDK_SPxK_1 | 485 | 491 | PF00069 | 0.749 |
MOD_CDK_SPxxK_3 | 485 | 492 | PF00069 | 0.751 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.605 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.660 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.640 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.544 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.160 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.423 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.363 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.497 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.527 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.368 |
MOD_Cter_Amidation | 475 | 478 | PF01082 | 0.680 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.365 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.620 |
MOD_GlcNHglycan | 243 | 247 | PF01048 | 0.433 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.284 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.441 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.524 |
MOD_GlcNHglycan | 314 | 318 | PF01048 | 0.496 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.407 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.730 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.714 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.693 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.495 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.670 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.367 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.629 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.311 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.650 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.594 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.648 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.206 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.440 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.476 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.376 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.468 |
MOD_PIKK_1 | 161 | 167 | PF00454 | 0.391 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.303 |
MOD_PK_1 | 108 | 114 | PF00069 | 0.432 |
MOD_PK_1 | 461 | 467 | PF00069 | 0.490 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.649 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.465 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.210 |
MOD_PKA_2 | 374 | 380 | PF00069 | 0.450 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.683 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.524 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.653 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.393 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.450 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.314 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.578 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.593 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.735 |
MOD_SUMO_rev_2 | 118 | 126 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 210 | 216 | PF00179 | 0.304 |
MOD_SUMO_rev_2 | 463 | 470 | PF00179 | 0.614 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.372 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.419 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.300 |
TRG_ER_diArg_1 | 324 | 326 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 329 | 331 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 373 | 376 | PF00400 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 478 | 482 | PF00026 | 0.649 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IL90 | Leptomonas seymouri | 59% | 98% |
A0A0S4IRI2 | Bodo saltans | 37% | 95% |
A0A1X0NR87 | Trypanosomatidae | 44% | 100% |
A0A3S7X1P4 | Leishmania donovani | 94% | 100% |
A0A422N7D8 | Trypanosoma rangeli | 42% | 100% |
A4HGR8 | Leishmania braziliensis | 81% | 100% |
A4I3U3 | Leishmania infantum | 94% | 100% |
D0A913 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B035 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
F4JRF4 | Arabidopsis thaliana | 34% | 80% |
O31584 | Bacillus subtilis (strain 168) | 31% | 100% |
P17802 | Escherichia coli (strain K12) | 31% | 100% |
P44320 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 29% | 100% |
P57617 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 25% | 100% |
P83847 | Geobacillus stearothermophilus | 34% | 100% |
Q05869 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 29% | 100% |
Q10159 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
Q8R5G2 | Rattus norvegicus | 30% | 97% |
Q99P21 | Mus musculus | 31% | 97% |
Q9UIF7 | Homo sapiens | 31% | 92% |
V5B3S1 | Trypanosoma cruzi | 41% | 100% |