Glycosylation, nucleoside phosphatase
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 | yes | yes: 4, no: 5 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4HUC4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009132 | nucleoside diphosphate metabolic process | 5 | 1 |
GO:0009134 | nucleoside diphosphate catabolic process | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019439 | aromatic compound catabolic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0046700 | heterocycle catabolic process | 4 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901292 | nucleoside phosphate catabolic process | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004382 | GDP phosphatase activity | 7 | 5 |
GO:0016462 | pyrophosphatase activity | 5 | 5 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 5 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 5 |
GO:0017110 | nucleoside diphosphate phosphatase activity | 6 | 5 |
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.258 |
CLV_C14_Caspase3-7 | 298 | 302 | PF00656 | 0.207 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.486 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.533 |
CLV_PCSK_PC1ET2_1 | 472 | 474 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 531 | 535 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.632 |
DEG_APCC_DBOX_1 | 132 | 140 | PF00400 | 0.457 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.447 |
DEG_SPOP_SBC_1 | 433 | 437 | PF00917 | 0.291 |
DOC_CYCLIN_yCln2_LP_2 | 532 | 538 | PF00134 | 0.315 |
DOC_MAPK_DCC_7 | 529 | 538 | PF00069 | 0.315 |
DOC_MAPK_gen_1 | 529 | 538 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 588 | 595 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 76 | 85 | PF00069 | 0.586 |
DOC_PP1_RVXF_1 | 408 | 415 | PF00149 | 0.279 |
DOC_PP4_MxPP_1 | 477 | 480 | PF00568 | 0.279 |
DOC_PP4_MxPP_1 | 551 | 554 | PF00568 | 0.291 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.254 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.336 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.291 |
DOC_USP7_UBL2_3 | 419 | 423 | PF12436 | 0.365 |
DOC_USP7_UBL2_3 | 505 | 509 | PF12436 | 0.207 |
DOC_USP7_UBL2_3 | 590 | 594 | PF12436 | 0.462 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.365 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 154 | 162 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 383 | 389 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 391 | 400 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.574 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.385 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.361 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 194 | 198 | PF00533 | 0.264 |
LIG_BRCT_BRCA1_1 | 565 | 569 | PF00533 | 0.340 |
LIG_deltaCOP1_diTrp_1 | 257 | 263 | PF00928 | 0.340 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.638 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.264 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.264 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.324 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.272 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.285 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.393 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.288 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.535 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.380 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.211 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.166 |
LIG_LIR_Gen_1 | 191 | 200 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 2 | 13 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 257 | 268 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 450 | 460 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 566 | 575 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 629 | 638 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 399 | 403 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 450 | 455 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 566 | 572 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 631 | 637 | PF02991 | 0.298 |
LIG_Pex14_2 | 5 | 9 | PF04695 | 0.442 |
LIG_Pex14_2 | 565 | 569 | PF04695 | 0.463 |
LIG_PTB_Apo_2 | 306 | 313 | PF02174 | 0.291 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.288 |
LIG_SH2_CRK | 635 | 639 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 194 | 198 | PF00017 | 0.288 |
LIG_SH2_NCK_1 | 646 | 650 | PF00017 | 0.327 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.264 |
LIG_SH2_SRC | 498 | 501 | PF00017 | 0.359 |
LIG_SH2_SRC | 637 | 640 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 194 | 198 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 384 | 388 | PF00017 | 0.291 |
LIG_SH2_STAP1 | 630 | 634 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 635 | 639 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 663 | 667 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.318 |
LIG_SH3_1 | 472 | 478 | PF00018 | 0.290 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.288 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.385 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.367 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.265 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.327 |
LIG_SUMO_SIM_anti_2 | 109 | 115 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 229 | 236 | PF11976 | 0.315 |
LIG_SUMO_SIM_anti_2 | 352 | 358 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 352 | 358 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 672 | 677 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 84 | 89 | PF11976 | 0.583 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.486 |
LIG_TRAF2_1 | 325 | 328 | PF00917 | 0.340 |
LIG_UBA3_1 | 166 | 175 | PF00899 | 0.563 |
LIG_UBA3_1 | 237 | 243 | PF00899 | 0.416 |
LIG_UBA3_1 | 290 | 295 | PF00899 | 0.340 |
LIG_UBA3_1 | 412 | 419 | PF00899 | 0.370 |
LIG_WRC_WIRS_1 | 564 | 569 | PF05994 | 0.237 |
LIG_WW_2 | 480 | 483 | PF00397 | 0.225 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.610 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.291 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.378 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.435 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.546 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.644 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.382 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.380 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.321 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.205 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.371 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.386 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.435 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.428 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.534 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.644 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.575 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.370 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.361 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.395 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.343 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.332 |
MOD_N-GLC_1 | 120 | 125 | PF02516 | 0.609 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.408 |
MOD_N-GLC_1 | 308 | 313 | PF02516 | 0.267 |
MOD_N-GLC_1 | 509 | 514 | PF02516 | 0.295 |
MOD_N-GLC_1 | 556 | 561 | PF02516 | 0.395 |
MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.145 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.545 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.574 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.279 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.451 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.267 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.354 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.327 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.287 |
MOD_NEK2_1 | 669 | 674 | PF00069 | 0.286 |
MOD_NEK2_2 | 622 | 627 | PF00069 | 0.391 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.605 |
MOD_PIKK_1 | 361 | 367 | PF00454 | 0.264 |
MOD_PIKK_1 | 417 | 423 | PF00454 | 0.327 |
MOD_PK_1 | 447 | 453 | PF00069 | 0.207 |
MOD_PKA_1 | 154 | 160 | PF00069 | 0.436 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.494 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.522 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.255 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.336 |
MOD_PKB_1 | 306 | 314 | PF00069 | 0.315 |
MOD_PKB_1 | 90 | 98 | PF00069 | 0.527 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.648 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.267 |
MOD_Plk_1 | 575 | 581 | PF00069 | 0.340 |
MOD_Plk_2-3 | 461 | 467 | PF00069 | 0.207 |
MOD_Plk_2-3 | 597 | 603 | PF00069 | 0.361 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.491 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.557 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.277 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.315 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.207 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.433 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.265 |
MOD_Plk_4 | 669 | 675 | PF00069 | 0.307 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.405 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.365 |
MOD_SUMO_for_1 | 626 | 629 | PF00179 | 0.375 |
MOD_SUMO_rev_2 | 55 | 62 | PF00179 | 0.391 |
MOD_SUMO_rev_2 | 587 | 596 | PF00179 | 0.327 |
TRG_DiLeu_BaEn_3 | 80 | 86 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_4 | 235 | 241 | PF01217 | 0.291 |
TRG_DiLeu_BaLyEn_6 | 528 | 533 | PF01217 | 0.340 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 639 | 642 | PF00928 | 0.377 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.580 |
TRG_NES_CRM1_1 | 105 | 119 | PF08389 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 289 | 294 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 97 | 101 | PF00026 | 0.616 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0E8 | Leptomonas seymouri | 46% | 99% |
A0A1X0NQR7 | Trypanosomatidae | 32% | 100% |
A0A3R7NV38 | Trypanosoma rangeli | 33% | 100% |
A0A3S7WR18 | Leishmania donovani | 99% | 100% |
A0JND9 | Bos taurus | 23% | 100% |
A4H5Z8 | Leishmania braziliensis | 70% | 100% |
C9ZVG6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AN23 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
P40009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
P49961 | Homo sapiens | 25% | 100% |
P55772 | Mus musculus | 24% | 100% |
Q28CF8 | Xenopus tropicalis | 21% | 100% |
Q3TCT4 | Mus musculus | 22% | 100% |
Q4QHK3 | Leishmania major | 90% | 100% |
Q5MY95 | Homo sapiens | 24% | 100% |
Q5REF6 | Pongo abelii | 21% | 100% |
Q8BFW6 | Mus musculus | 26% | 100% |
Q8TGH6 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 30% | 100% |
Q9HEM6 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 31% | 100% |
Q9NQZ7 | Homo sapiens | 21% | 100% |