Phosphodiesterase, with probable N-terminal lipidation signal. Not embedded in membrane, like its homologs.
Phosphodiesterase, cAMP phosphodiesterase A PDEA
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 2 |
Forrest at al. (procyclic) | yes | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HXY3
Term | Name | Level | Count |
---|---|---|---|
GO:0007165 | signal transduction | 2 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0050789 | regulation of biological process | 2 | 13 |
GO:0050794 | regulation of cellular process | 3 | 13 |
GO:0065007 | biological regulation | 1 | 13 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:2000377 | regulation of reactive oxygen species metabolic process | 5 | 1 |
GO:2000378 | negative regulation of reactive oxygen species metabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004112 | cyclic-nucleotide phosphodiesterase activity | 6 | 13 |
GO:0004114 | 3',5'-cyclic-nucleotide phosphodiesterase activity | 7 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 13 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.619 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 126 | 128 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 408 | 410 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.373 |
DEG_APCC_DBOX_1 | 408 | 416 | PF00400 | 0.426 |
DEG_APCC_DBOX_1 | 452 | 460 | PF00400 | 0.420 |
DEG_SCF_FBW7_2 | 596 | 602 | PF00400 | 0.522 |
DOC_CKS1_1 | 596 | 601 | PF01111 | 0.522 |
DOC_CYCLIN_RxL_1 | 565 | 575 | PF00134 | 0.441 |
DOC_MAPK_gen_1 | 251 | 261 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.609 |
DOC_PIKK_1 | 451 | 459 | PF02985 | 0.468 |
DOC_PP4_FxxP_1 | 429 | 432 | PF00568 | 0.468 |
DOC_SPAK_OSR1_1 | 612 | 616 | PF12202 | 0.500 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.281 |
DOC_USP7_UBL2_3 | 196 | 200 | PF12436 | 0.634 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.496 |
LIG_14-3-3_CanoR_1 | 127 | 131 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 134 | 142 | PF00244 | 0.529 |
LIG_APCC_ABBA_1 | 597 | 602 | PF00400 | 0.402 |
LIG_BRCT_BRCA1_1 | 461 | 465 | PF00533 | 0.402 |
LIG_BRCT_BRCA1_1 | 556 | 560 | PF00533 | 0.386 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.510 |
LIG_deltaCOP1_diTrp_1 | 314 | 321 | PF00928 | 0.425 |
LIG_deltaCOP1_diTrp_1 | 69 | 74 | PF00928 | 0.496 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.553 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.586 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.373 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.740 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.557 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.610 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.594 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.381 |
LIG_FXI_DFP_1 | 426 | 430 | PF00024 | 0.500 |
LIG_IBAR_NPY_1 | 382 | 384 | PF08397 | 0.420 |
LIG_LIR_Apic_2 | 266 | 271 | PF02991 | 0.554 |
LIG_LIR_Apic_2 | 428 | 432 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 255 | 264 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 347 | 357 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 462 | 473 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 598 | 609 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 69 | 77 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 598 | 604 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 69 | 73 | PF02991 | 0.429 |
LIG_MLH1_MIPbox_1 | 70 | 74 | PF16413 | 0.511 |
LIG_Pex14_1 | 70 | 74 | PF04695 | 0.417 |
LIG_Pex14_2 | 357 | 361 | PF04695 | 0.440 |
LIG_PTB_Apo_2 | 467 | 474 | PF02174 | 0.420 |
LIG_REV1ctd_RIR_1 | 71 | 79 | PF16727 | 0.562 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.422 |
LIG_SH2_GRB2like | 384 | 387 | PF00017 | 0.373 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.663 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.373 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.468 |
LIG_Sin3_3 | 256 | 263 | PF02671 | 0.527 |
LIG_SUMO_SIM_anti_2 | 21 | 26 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.626 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.644 |
LIG_TRAF2_1 | 31 | 34 | PF00917 | 0.649 |
LIG_UBA3_1 | 164 | 171 | PF00899 | 0.627 |
LIG_UBA3_1 | 260 | 265 | PF00899 | 0.421 |
LIG_WRC_WIRS_1 | 476 | 481 | PF05994 | 0.441 |
MOD_CDK_SPxxK_3 | 275 | 282 | PF00069 | 0.622 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.699 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.553 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.462 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.591 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.516 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.504 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.589 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.575 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.405 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.364 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.366 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.407 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.689 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.414 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.574 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.523 |
MOD_GlcNHglycan | 372 | 375 | PF01048 | 0.486 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.483 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.586 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.679 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.683 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.445 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.494 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.450 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.403 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.523 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.522 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.597 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.491 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.677 |
MOD_LATS_1 | 439 | 445 | PF00433 | 0.402 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.645 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.644 |
MOD_N-GLC_2 | 527 | 529 | PF02516 | 0.524 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.635 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.451 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.588 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.535 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.333 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.389 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.500 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.446 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.468 |
MOD_NEK2_2 | 384 | 389 | PF00069 | 0.386 |
MOD_NEK2_2 | 445 | 450 | PF00069 | 0.420 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.618 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.621 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.503 |
MOD_PIKK_1 | 585 | 591 | PF00454 | 0.481 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.597 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.550 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.535 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.375 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.647 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.589 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.584 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.492 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.403 |
MOD_Plk_1 | 515 | 521 | PF00069 | 0.508 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.577 |
MOD_Plk_2-3 | 133 | 139 | PF00069 | 0.610 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.447 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.581 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.409 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.424 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.416 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.511 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.416 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.191 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.373 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.521 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.619 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.573 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.567 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.373 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.496 |
MOD_SUMO_rev_2 | 105 | 111 | PF00179 | 0.734 |
MOD_SUMO_rev_2 | 619 | 623 | PF00179 | 0.591 |
TRG_DiLeu_BaEn_2 | 572 | 578 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.259 |
TRG_NES_CRM1_1 | 606 | 620 | PF08389 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.652 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 568 | 573 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Y4 | Leptomonas seymouri | 34% | 89% |
A0A0N1PG81 | Leptomonas seymouri | 66% | 100% |
A0A0S4KIW5 | Bodo saltans | 47% | 100% |
A0A1X0P701 | Trypanosomatidae | 50% | 100% |
A0A3Q8IB14 | Leishmania donovani | 99% | 100% |
A0A422P0P1 | Trypanosoma rangeli | 49% | 100% |
A4H9L9 | Leishmania braziliensis | 86% | 100% |
D0A5C4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9ARP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q6S998 | Leishmania major | 96% | 100% |
V5BNN7 | Trypanosoma cruzi | 46% | 100% |