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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HAS9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006281 | DNA repair | 5 | 11 |
GO:0006284 | base-excision repair | 6 | 10 |
GO:0006289 | nucleotide-excision repair | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0006285 | base-excision repair, AP site formation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000702 | oxidized base lesion DNA N-glycosylase activity | 5 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0003684 | damaged DNA binding | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003906 | DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008534 | oxidized purine nucleobase lesion DNA N-glycosylase activity | 6 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 11 |
GO:0016799 | hydrolase activity, hydrolyzing N-glycosyl compounds | 4 | 11 |
GO:0016829 | lyase activity | 2 | 11 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 11 |
GO:0019104 | DNA N-glycosylase activity | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0140078 | class I DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 11 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0034039 | 8-oxo-7,8-dihydroguanine DNA N-glycosylase activity | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.405 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.743 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.362 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 469 | 471 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 88 | 90 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.376 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.405 |
DEG_APCC_DBOX_1 | 414 | 422 | PF00400 | 0.482 |
DEG_SCF_FBW7_1 | 134 | 141 | PF00400 | 0.405 |
DEG_SCF_FBW7_1 | 275 | 281 | PF00400 | 0.405 |
DEG_SCF_FBW7_1 | 42 | 47 | PF00400 | 0.492 |
DEG_SIAH_1 | 459 | 467 | PF03145 | 0.466 |
DEG_SPOP_SBC_1 | 17 | 21 | PF00917 | 0.574 |
DEG_SPOP_SBC_1 | 505 | 509 | PF00917 | 0.467 |
DOC_CKS1_1 | 135 | 140 | PF01111 | 0.405 |
DOC_CKS1_1 | 275 | 280 | PF01111 | 0.405 |
DOC_CKS1_1 | 41 | 46 | PF01111 | 0.558 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 25 | 32 | PF00134 | 0.405 |
DOC_MAPK_gen_1 | 23 | 32 | PF00069 | 0.583 |
DOC_MAPK_gen_1 | 426 | 434 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 468 | 478 | PF00069 | 0.507 |
DOC_MAPK_JIP1_4 | 472 | 478 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 216 | 225 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 23 | 32 | PF00069 | 0.586 |
DOC_MAPK_NFAT4_5 | 25 | 33 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 342 | 349 | PF00149 | 0.482 |
DOC_PP2B_LxvP_1 | 419 | 422 | PF13499 | 0.496 |
DOC_PP4_MxPP_1 | 381 | 384 | PF00568 | 0.405 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.524 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 16 | 26 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 518 | 523 | PF00244 | 0.746 |
LIG_Actin_WH2_1 | 45 | 62 | PF00022 | 0.586 |
LIG_Actin_WH2_2 | 44 | 62 | PF00022 | 0.475 |
LIG_BIR_III_4 | 319 | 323 | PF00653 | 0.405 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.535 |
LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.562 |
LIG_BRCT_BRCA1_1 | 559 | 563 | PF00533 | 0.364 |
LIG_CtBP_PxDLS_1 | 148 | 152 | PF00389 | 0.405 |
LIG_deltaCOP1_diTrp_1 | 172 | 178 | PF00928 | 0.562 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.556 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.499 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.471 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.590 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.551 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.525 |
LIG_LIR_Apic_2 | 325 | 330 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 162 | 171 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 220 | 228 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 545 | 555 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 328 | 332 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 545 | 550 | PF02991 | 0.553 |
LIG_MYND_1 | 309 | 313 | PF01753 | 0.502 |
LIG_MYND_2 | 2 | 6 | PF01753 | 0.530 |
LIG_NRBOX | 199 | 205 | PF00104 | 0.405 |
LIG_Pex14_1 | 323 | 327 | PF04695 | 0.562 |
LIG_Pex14_2 | 110 | 114 | PF04695 | 0.433 |
LIG_Pex14_2 | 547 | 551 | PF04695 | 0.392 |
LIG_PTB_Apo_2 | 394 | 401 | PF02174 | 0.586 |
LIG_PTB_Phospho_1 | 394 | 400 | PF10480 | 0.586 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.405 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.586 |
LIG_SH2_CRK | 400 | 404 | PF00017 | 0.586 |
LIG_SH2_PTP2 | 222 | 225 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 400 | 404 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 261 | 264 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.450 |
LIG_SH3_1 | 528 | 534 | PF00018 | 0.635 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.562 |
LIG_SH3_3 | 528 | 534 | PF00018 | 0.594 |
LIG_SUMO_SIM_anti_2 | 416 | 422 | PF11976 | 0.586 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.564 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.560 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.405 |
LIG_TYR_ITIM | 115 | 120 | PF00017 | 0.562 |
LIG_WRC_WIRS_1 | 236 | 241 | PF05994 | 0.447 |
LIG_WW_1 | 533 | 536 | PF00397 | 0.586 |
LIG_WW_3 | 522 | 526 | PF00397 | 0.582 |
MOD_CDK_SPK_2 | 40 | 45 | PF00069 | 0.496 |
MOD_CDK_SPK_2 | 456 | 461 | PF00069 | 0.612 |
MOD_CDK_SPxK_1 | 274 | 280 | PF00069 | 0.518 |
MOD_CDK_SPxxK_3 | 178 | 185 | PF00069 | 0.586 |
MOD_CDK_SPxxK_3 | 305 | 312 | PF00069 | 0.558 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.553 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.586 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.405 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.542 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.506 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.746 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.614 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.541 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.513 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.469 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.486 |
MOD_CMANNOS | 175 | 178 | PF00535 | 0.282 |
MOD_Cter_Amidation | 424 | 427 | PF01082 | 0.282 |
MOD_Cter_Amidation | 466 | 469 | PF01082 | 0.740 |
MOD_Cter_Amidation | 86 | 89 | PF01082 | 0.205 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.386 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.211 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.799 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.637 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.382 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.481 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.570 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.508 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.574 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.556 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.534 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.567 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.426 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.487 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.553 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.313 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.362 |
MOD_N-GLC_1 | 437 | 442 | PF02516 | 0.386 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.367 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.519 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.550 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.479 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.468 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.519 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.589 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.463 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.569 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.465 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.405 |
MOD_NEK2_2 | 322 | 327 | PF00069 | 0.405 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.482 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.567 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.502 |
MOD_PKA_1 | 295 | 301 | PF00069 | 0.468 |
MOD_PKA_1 | 468 | 474 | PF00069 | 0.644 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.496 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.572 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.391 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.484 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.756 |
MOD_Plk_1 | 245 | 251 | PF00069 | 0.562 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.591 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.405 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.574 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.536 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.444 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.562 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.492 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.482 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.482 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.361 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.568 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.585 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.518 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.558 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.514 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.496 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.508 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.656 |
MOD_SUMO_rev_2 | 281 | 290 | PF00179 | 0.522 |
TRG_ENDOCYTIC_2 | 117 | 120 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 470 | 473 | PF00400 | 0.668 |
TRG_NES_CRM1_1 | 159 | 172 | PF08389 | 0.586 |
TRG_NLS_MonoExtC_3 | 467 | 472 | PF00514 | 0.656 |
TRG_NLS_MonoExtN_4 | 465 | 472 | PF00514 | 0.617 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I223 | Leptomonas seymouri | 43% | 97% |
A0A1X0P9L2 | Trypanosomatidae | 29% | 100% |
A0A3R7MS38 | Trypanosoma rangeli | 33% | 100% |
A0A3S7X7Y5 | Leishmania donovani | 69% | 100% |
A4I9Y9 | Leishmania infantum | 69% | 100% |
C9ZMN9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B503 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4Q2Y3 | Leishmania major | 70% | 100% |
V5BKI1 | Trypanosoma cruzi | 31% | 100% |