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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: A0A3S7X1H5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 4 |
GO:0006259 | DNA metabolic process | 4 | 4 |
GO:0006281 | DNA repair | 5 | 4 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0006950 | response to stress | 2 | 4 |
GO:0006974 | DNA damage response | 4 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0033554 | cellular response to stress | 3 | 4 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 4 |
GO:0046483 | heterocycle metabolic process | 3 | 4 |
GO:0050896 | response to stimulus | 1 | 4 |
GO:0051716 | cellular response to stimulus | 2 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:0090304 | nucleic acid metabolic process | 4 | 4 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 4 |
GO:0006260 | DNA replication | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 4 |
GO:0003677 | DNA binding | 4 | 4 |
GO:0003684 | damaged DNA binding | 5 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
GO:0016779 | nucleotidyltransferase activity | 4 | 2 |
GO:0034061 | DNA polymerase activity | 4 | 2 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.562 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.808 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.808 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 532 | 534 | PF00082 | 0.571 |
CLV_PCSK_PC7_1 | 528 | 534 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.546 |
DEG_ODPH_VHL_1 | 444 | 456 | PF01847 | 0.501 |
DOC_MAPK_DCC_7 | 282 | 291 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 272 | 281 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 282 | 291 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 274 | 283 | PF00069 | 0.574 |
DOC_MAPK_MEF2A_6 | 77 | 84 | PF00069 | 0.600 |
DOC_PP1_RVXF_1 | 226 | 233 | PF00149 | 0.541 |
DOC_PP2B_LxvP_1 | 509 | 512 | PF13499 | 0.496 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.499 |
DOC_USP7_UBL2_3 | 187 | 191 | PF12436 | 0.614 |
DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.698 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 494 | 499 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 210 | 219 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 354 | 359 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 420 | 426 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 492 | 498 | PF00244 | 0.607 |
LIG_14-3-3_CterR_2 | 533 | 536 | PF00244 | 0.570 |
LIG_Actin_WH2_2 | 161 | 179 | PF00022 | 0.636 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.433 |
LIG_BIR_III_2 | 404 | 408 | PF00653 | 0.560 |
LIG_BRCT_BRCA1_1 | 235 | 239 | PF00533 | 0.594 |
LIG_BRCT_BRCA1_1 | 417 | 421 | PF00533 | 0.507 |
LIG_CtBP_PxDLS_1 | 391 | 395 | PF00389 | 0.525 |
LIG_EVH1_2 | 468 | 472 | PF00568 | 0.425 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.603 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.544 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.622 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.489 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.539 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 40 | 50 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.582 |
LIG_MYND_1 | 507 | 511 | PF01753 | 0.496 |
LIG_OCRL_FandH_1 | 268 | 280 | PF00620 | 0.480 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.465 |
LIG_SH3_2 | 487 | 492 | PF14604 | 0.569 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.638 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.576 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.529 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.604 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.560 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.540 |
LIG_SH3_4 | 52 | 59 | PF00018 | 0.603 |
LIG_SUMO_SIM_par_1 | 57 | 63 | PF11976 | 0.616 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.551 |
LIG_TRAF2_1 | 63 | 66 | PF00917 | 0.622 |
LIG_TRFH_1 | 442 | 446 | PF08558 | 0.521 |
MOD_CDK_SPxxK_3 | 485 | 492 | PF00069 | 0.568 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.628 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.416 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.532 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.581 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.520 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.554 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.714 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.542 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.623 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.604 |
MOD_Cter_Amidation | 293 | 296 | PF01082 | 0.766 |
MOD_Cter_Amidation | 352 | 355 | PF01082 | 0.554 |
MOD_DYRK1A_RPxSP_1 | 427 | 431 | PF00069 | 0.499 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.772 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.619 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.492 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.595 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.553 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.621 |
MOD_GlcNHglycan | 371 | 375 | PF01048 | 0.631 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.609 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.548 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.760 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.639 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.346 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.535 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.581 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.528 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.506 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.524 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.519 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.565 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.565 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.505 |
MOD_LATS_1 | 208 | 214 | PF00433 | 0.427 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.594 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.549 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.526 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.560 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.542 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.519 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.585 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.413 |
MOD_NEK2_2 | 94 | 99 | PF00069 | 0.555 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.405 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.611 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.536 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.493 |
MOD_PKA_1 | 190 | 196 | PF00069 | 0.487 |
MOD_PKA_1 | 354 | 360 | PF00069 | 0.552 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.727 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.652 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.551 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.503 |
MOD_Plk_1 | 113 | 119 | PF00069 | 0.571 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.485 |
MOD_Plk_2-3 | 399 | 405 | PF00069 | 0.559 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.416 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.554 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.732 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.616 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.425 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.506 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.563 |
MOD_ProDKin_1 | 494 | 500 | PF00069 | 0.541 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.499 |
TRG_DiLeu_BaLyEn_6 | 274 | 279 | PF01217 | 0.593 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.430 |
TRG_NES_CRM1_1 | 66 | 78 | PF08389 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 210 | 214 | PF00026 | 0.550 |