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 | 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: Q4Q2Y3
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:0006285 | base-excision repair, AP site formation | 5 | 2 |
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:0006284 | base-excision repair | 6 | 9 |
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:0034039 | 8-oxo-7,8-dihydroguanine DNA N-glycosylase activity | 7 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 173 | 177 | PF00656 | 0.451 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 180 | 182 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.222 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 488 | 490 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.332 |
CLV_PCSK_FUR_1 | 82 | 86 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.195 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 465 | 467 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.259 |
CLV_PCSK_PC7_1 | 82 | 88 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.311 |
DEG_APCC_DBOX_1 | 410 | 418 | PF00400 | 0.436 |
DEG_SCF_FBW7_1 | 6 | 11 | PF00400 | 0.389 |
DEG_SPOP_SBC_1 | 14 | 18 | PF00917 | 0.410 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.539 |
DOC_CKS1_1 | 38 | 43 | PF01111 | 0.525 |
DOC_CYCLIN_RxL_1 | 156 | 166 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 193 | 201 | PF00134 | 0.515 |
DOC_CYCLIN_RxL_1 | 337 | 348 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 119 | 125 | PF00134 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 217 | 223 | PF00134 | 0.451 |
DOC_MAPK_gen_1 | 20 | 29 | PF00069 | 0.567 |
DOC_MAPK_gen_1 | 371 | 379 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 39 | 48 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 422 | 430 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 479 | 486 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 489 | 497 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 159 | 167 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 20 | 27 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 338 | 345 | PF00149 | 0.436 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.451 |
DOC_PP2B_LxvP_1 | 362 | 365 | PF13499 | 0.404 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 453 | 456 | PF13499 | 0.424 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.496 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.486 |
LIG_14-3-3_CanoR_1 | 13 | 23 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 159 | 164 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.504 |
LIG_Actin_WH2_1 | 42 | 59 | PF00022 | 0.482 |
LIG_Actin_WH2_2 | 41 | 59 | PF00022 | 0.420 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.531 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.420 |
LIG_BRCT_BRCA1_1 | 555 | 559 | PF00533 | 0.308 |
LIG_deltaCOP1_diTrp_1 | 168 | 174 | PF00928 | 0.531 |
LIG_deltaCOP1_diTrp_1 | 318 | 325 | PF00928 | 0.523 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.537 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.501 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.470 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.436 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.539 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.447 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.556 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.389 |
LIG_LIR_Apic_2 | 321 | 326 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 158 | 167 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 318 | 326 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 107 | 113 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 11 | 15 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 318 | 322 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.560 |
LIG_MYND_1 | 305 | 309 | PF01753 | 0.435 |
LIG_MYND_2 | 380 | 384 | PF01753 | 0.451 |
LIG_Pex14_1 | 319 | 323 | PF04695 | 0.531 |
LIG_Pex14_2 | 543 | 547 | PF04695 | 0.340 |
LIG_PTB_Apo_2 | 390 | 397 | PF02174 | 0.482 |
LIG_PTB_Phospho_1 | 390 | 396 | PF10480 | 0.482 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.482 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.435 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.482 |
LIG_SH2_PTP2 | 218 | 221 | PF00017 | 0.531 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.439 |
LIG_SH2_STAT3 | 405 | 408 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 452 | 455 | PF00017 | 0.369 |
LIG_SH3_1 | 466 | 472 | PF00018 | 0.497 |
LIG_SH3_1 | 524 | 530 | PF00018 | 0.600 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.531 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.512 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.543 |
LIG_SUMO_SIM_anti_2 | 412 | 418 | PF11976 | 0.482 |
LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.529 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.667 |
LIG_TRAF2_1 | 508 | 511 | PF00917 | 0.528 |
LIG_TYR_ITIM | 111 | 116 | PF00017 | 0.531 |
LIG_WRC_WIRS_1 | 232 | 237 | PF05994 | 0.438 |
LIG_WW_1 | 529 | 532 | PF00397 | 0.527 |
MOD_CDK_SPK_2 | 37 | 42 | PF00069 | 0.449 |
MOD_CDK_SPxxK_3 | 174 | 181 | PF00069 | 0.482 |
MOD_CDK_SPxxK_3 | 301 | 308 | PF00069 | 0.466 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.501 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.482 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.502 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.638 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.476 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.648 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.545 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.434 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.498 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.424 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.577 |
MOD_CMANNOS | 171 | 174 | PF00535 | 0.236 |
MOD_Cter_Amidation | 420 | 423 | PF01082 | 0.236 |
MOD_Cter_Amidation | 462 | 465 | PF01082 | 0.622 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.238 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.349 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.345 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.201 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.307 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.622 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.727 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.544 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.507 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.464 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.513 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.529 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.521 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.501 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.480 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.466 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.444 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.420 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.473 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.334 |
MOD_N-GLC_1 | 433 | 438 | PF02516 | 0.282 |
MOD_N-GLC_2 | 103 | 105 | PF02516 | 0.181 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.659 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.503 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.501 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.428 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.418 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.435 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.492 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.482 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.542 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.561 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.551 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.436 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.482 |
MOD_PIKK_1 | 72 | 78 | PF00454 | 0.435 |
MOD_PKA_1 | 298 | 304 | PF00069 | 0.552 |
MOD_PKA_1 | 464 | 470 | PF00069 | 0.585 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.527 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.449 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.495 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.425 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.484 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.659 |
MOD_PKB_1 | 85 | 93 | PF00069 | 0.389 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.534 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.550 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.482 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.531 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.476 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.470 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.351 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.544 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.482 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.466 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.449 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.464 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.515 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.630 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.486 |
MOD_SUMO_rev_2 | 366 | 373 | PF00179 | 0.490 |
TRG_DiLeu_BaEn_2 | 352 | 358 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 123 | 126 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 466 | 469 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 561 | 564 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.430 |
TRG_NES_CRM1_1 | 155 | 168 | PF08389 | 0.482 |
TRG_NLS_MonoCore_2 | 83 | 88 | PF00514 | 0.389 |
TRG_NLS_MonoExtC_3 | 463 | 468 | PF00514 | 0.602 |
TRG_NLS_MonoExtN_4 | 464 | 469 | PF00514 | 0.595 |
TRG_NLS_MonoExtN_4 | 82 | 88 | PF00514 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 159 | 164 | PF00026 | 0.317 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I223 | Leptomonas seymouri | 45% | 96% |
A0A1X0P9L2 | Trypanosomatidae | 32% | 100% |
A0A3R7MS38 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X7Y5 | Leishmania donovani | 87% | 100% |
A4HAS9 | Leishmania braziliensis | 70% | 99% |
A4I9Y9 | Leishmania infantum | 87% | 100% |
C9ZMN9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9B503 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5BKI1 | Trypanosoma cruzi | 33% | 100% |