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: A0A3S7X7Y5
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 | 173 | 177 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 297 | 301 | PF00656 | 0.559 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.362 |
CLV_PCSK_FUR_1 | 82 | 86 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.386 |
DEG_APCC_DBOX_1 | 410 | 418 | PF00400 | 0.482 |
DEG_SPOP_SBC_1 | 133 | 137 | PF00917 | 0.447 |
DEG_SPOP_SBC_1 | 14 | 18 | PF00917 | 0.549 |
DOC_CKS1_1 | 38 | 43 | PF01111 | 0.558 |
DOC_CYCLIN_RxL_1 | 156 | 166 | PF00134 | 0.553 |
DOC_CYCLIN_RxL_1 | 337 | 348 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 119 | 125 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 217 | 223 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 20 | 29 | PF00069 | 0.583 |
DOC_MAPK_gen_1 | 422 | 430 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 489 | 497 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 159 | 167 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 20 | 27 | PF00069 | 0.586 |
DOC_PP1_RVXF_1 | 338 | 345 | PF00149 | 0.482 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.530 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.496 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.529 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.587 |
DOC_USP7_UBL2_3 | 370 | 374 | PF12436 | 0.525 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.619 |
LIG_14-3-3_CanoR_1 | 159 | 164 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 513 | 520 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 9 | 13 | PF00244 | 0.573 |
LIG_Actin_WH2_1 | 42 | 59 | PF00022 | 0.586 |
LIG_Actin_WH2_2 | 187 | 202 | PF00022 | 0.433 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.562 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.361 |
LIG_deltaCOP1_diTrp_1 | 168 | 174 | PF00928 | 0.562 |
LIG_deltaCOP1_diTrp_1 | 318 | 325 | PF00928 | 0.557 |
LIG_deltaCOP1_diTrp_1 | 541 | 547 | PF00928 | 0.509 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.530 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.526 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.513 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.482 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.539 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.542 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.587 |
LIG_LIR_Apic_2 | 321 | 326 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 158 | 167 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 316 | 326 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 11 | 15 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.487 |
LIG_MYND_2 | 380 | 384 | PF01753 | 0.530 |
LIG_Pex14_1 | 319 | 323 | PF04695 | 0.562 |
LIG_Pex14_2 | 543 | 547 | PF04695 | 0.389 |
LIG_PTB_Apo_2 | 338 | 345 | PF02174 | 0.405 |
LIG_PTB_Apo_2 | 390 | 397 | PF02174 | 0.586 |
LIG_PTB_Phospho_1 | 390 | 396 | PF10480 | 0.586 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.586 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.502 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.586 |
LIG_SH2_PTP2 | 218 | 221 | PF00017 | 0.562 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 405 | 408 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.429 |
LIG_SH3_1 | 524 | 530 | PF00018 | 0.591 |
LIG_SH3_1 | 72 | 78 | PF00018 | 0.433 |
LIG_SH3_2 | 77 | 82 | PF14604 | 0.433 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.553 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.551 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.582 |
LIG_SUMO_SIM_anti_2 | 412 | 418 | PF11976 | 0.586 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.560 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.708 |
LIG_TRAF2_1 | 508 | 511 | PF00917 | 0.577 |
LIG_TYR_ITIM | 111 | 116 | PF00017 | 0.562 |
LIG_TYR_ITIM | 558 | 563 | PF00017 | 0.482 |
LIG_WRC_WIRS_1 | 232 | 237 | PF05994 | 0.447 |
LIG_WW_1 | 529 | 532 | PF00397 | 0.566 |
MOD_CDK_SPK_2 | 37 | 42 | PF00069 | 0.496 |
MOD_CDK_SPxxK_3 | 174 | 181 | PF00069 | 0.586 |
MOD_CDK_SPxxK_3 | 301 | 308 | PF00069 | 0.558 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.553 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.586 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.538 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.540 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.542 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.696 |
MOD_CK1_1 | 515 | 521 | PF00069 | 0.652 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.566 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.541 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.591 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.588 |
MOD_CMANNOS | 171 | 174 | PF00535 | 0.282 |
MOD_Cter_Amidation | 420 | 423 | PF01082 | 0.282 |
MOD_Cter_Amidation | 462 | 465 | PF01082 | 0.733 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.347 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.291 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.330 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.386 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.240 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.330 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.619 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.706 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.233 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.385 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.571 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.547 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.508 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.540 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.556 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.528 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.516 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.539 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.502 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.426 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.476 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.541 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.519 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.362 |
MOD_N-GLC_1 | 433 | 438 | PF02516 | 0.386 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.676 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.522 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.523 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.499 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.465 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.534 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.482 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.586 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.542 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.600 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.565 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.482 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.458 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.586 |
MOD_PKA_1 | 464 | 470 | PF00069 | 0.638 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.497 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.526 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.490 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.537 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.496 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.651 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.703 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.523 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.562 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.532 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.586 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.562 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.486 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.482 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.508 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.353 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.570 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.585 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.558 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.496 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.579 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.573 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.612 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.608 |
TRG_DiLeu_BaEn_2 | 352 | 358 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.407 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 466 | 469 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 561 | 564 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.503 |
TRG_NES_CRM1_1 | 155 | 168 | PF08389 | 0.586 |
TRG_NLS_MonoExtC_3 | 463 | 468 | PF00514 | 0.653 |
TRG_NLS_MonoExtN_4 | 464 | 469 | PF00514 | 0.649 |
TRG_Pf-PMV_PEXEL_1 | 159 | 164 | PF00026 | 0.353 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I223 | Leptomonas seymouri | 46% | 96% |
A0A1X0P9L2 | Trypanosomatidae | 31% | 100% |
A0A3R7MS38 | Trypanosoma rangeli | 35% | 100% |
A4HAS9 | Leishmania braziliensis | 69% | 100% |
A4I9Y9 | Leishmania infantum | 99% | 100% |
C9ZMN9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9B503 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q2Y3 | Leishmania major | 87% | 100% |
V5BKI1 | Trypanosoma cruzi | 34% | 100% |