Phosphodiesterase, with probable N-terminal lipidation signal. Not embedded in membrane, like its homologs.
Phosphodiesterase, 3'5'-cyclic nucleotide phosphodiesterase
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) | yes | yes: 3 |
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: 7 |
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:0020016 | ciliary pocket | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0016020 | membrane | 2 | 3 |
Related structures:
AlphaFold database: A4I4V8
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 |
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 | 184 | 188 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.634 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 706 | 708 | PF00082 | 0.612 |
CLV_PCSK_PC7_1 | 300 | 306 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 582 | 586 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.509 |
CLV_Separin_Metazoa | 543 | 547 | PF03568 | 0.416 |
DEG_APCC_DBOX_1 | 445 | 453 | PF00400 | 0.471 |
DEG_SCF_FBW7_1 | 13 | 20 | PF00400 | 0.711 |
DEG_SPOP_SBC_1 | 76 | 80 | PF00917 | 0.691 |
DOC_CYCLIN_RxL_1 | 643 | 653 | PF00134 | 0.461 |
DOC_MAPK_gen_1 | 446 | 452 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 600 | 608 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 646 | 652 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 600 | 608 | PF00069 | 0.350 |
DOC_PP4_FxxP_1 | 117 | 120 | PF00568 | 0.522 |
DOC_PP4_FxxP_1 | 204 | 207 | PF00568 | 0.576 |
DOC_PP4_FxxP_1 | 506 | 509 | PF00568 | 0.377 |
DOC_SPAK_OSR1_1 | 224 | 228 | PF12202 | 0.497 |
DOC_SPAK_OSR1_1 | 447 | 451 | PF12202 | 0.528 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.496 |
DOC_USP7_MATH_2 | 347 | 353 | PF00917 | 0.562 |
DOC_USP7_UBL2_3 | 632 | 636 | PF12436 | 0.497 |
DOC_USP7_UBL2_3 | 86 | 90 | PF12436 | 0.574 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 650 | 655 | PF00397 | 0.348 |
LIG_14-3-3_CanoR_1 | 140 | 147 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 590 | 597 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 605 | 611 | PF00244 | 0.395 |
LIG_APCC_ABBA_1 | 114 | 119 | PF00400 | 0.537 |
LIG_APCC_ABBA_1 | 652 | 657 | PF00400 | 0.377 |
LIG_BRCT_BRCA1_1 | 634 | 638 | PF00533 | 0.395 |
LIG_CSL_BTD_1 | 335 | 338 | PF09270 | 0.703 |
LIG_CtBP_PxDLS_1 | 207 | 211 | PF00389 | 0.590 |
LIG_eIF4E_1 | 423 | 429 | PF01652 | 0.411 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.432 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.547 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.487 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.522 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.622 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.445 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.294 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.475 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.503 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.776 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.770 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.467 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.582 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.407 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.326 |
LIG_IBAR_NPY_1 | 459 | 461 | PF08397 | 0.427 |
LIG_IRF3_LxIS_1 | 648 | 653 | PF10401 | 0.446 |
LIG_LIR_Apic_2 | 201 | 207 | PF02991 | 0.588 |
LIG_LIR_Apic_2 | 505 | 509 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 187 | 198 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 394 | 402 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 406 | 415 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 424 | 434 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 541 | 550 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 159 | 163 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 199 | 205 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 406 | 410 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 492 | 498 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 541 | 545 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 671 | 675 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.568 |
LIG_LYPXL_yS_3 | 202 | 205 | PF13949 | 0.515 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.400 |
LIG_PTB_Apo_2 | 544 | 551 | PF02174 | 0.443 |
LIG_PTB_Apo_2 | 698 | 705 | PF02174 | 0.560 |
LIG_PTB_Phospho_1 | 544 | 550 | PF10480 | 0.443 |
LIG_PTB_Phospho_1 | 698 | 704 | PF10480 | 0.560 |
LIG_Rb_pABgroove_1 | 317 | 325 | PF01858 | 0.665 |
LIG_REV1ctd_RIR_1 | 161 | 169 | PF16727 | 0.398 |
LIG_SH2_CRK | 407 | 411 | PF00017 | 0.428 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.564 |
LIG_SH2_GRB2like | 437 | 440 | PF00017 | 0.520 |
LIG_SH2_GRB2like | 461 | 464 | PF00017 | 0.361 |
LIG_SH2_NCK_1 | 236 | 240 | PF00017 | 0.587 |
LIG_SH2_NCK_1 | 407 | 411 | PF00017 | 0.429 |
LIG_SH2_SRC | 323 | 326 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 138 | 142 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 423 | 427 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 627 | 631 | PF00017 | 0.416 |
LIG_SH2_STAT3 | 675 | 678 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 675 | 678 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.448 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.745 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.560 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.451 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.771 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.741 |
LIG_SH3_3 | 683 | 689 | PF00018 | 0.421 |
LIG_SUMO_SIM_anti_2 | 682 | 688 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 448 | 454 | PF11976 | 0.512 |
LIG_TRAF2_1 | 143 | 146 | PF00917 | 0.541 |
LIG_TRAF2_1 | 342 | 345 | PF00917 | 0.556 |
LIG_TRAF2_1 | 490 | 493 | PF00917 | 0.395 |
LIG_TRFH_1 | 359 | 363 | PF08558 | 0.449 |
LIG_TYR_ITIM | 435 | 440 | PF00017 | 0.524 |
LIG_TYR_ITSM | 422 | 429 | PF00017 | 0.423 |
LIG_WRC_WIRS_1 | 350 | 355 | PF05994 | 0.455 |
LIG_WRC_WIRS_1 | 690 | 695 | PF05994 | 0.419 |
MOD_CDK_SPxxK_3 | 213 | 220 | PF00069 | 0.546 |
MOD_CDK_SPxxK_3 | 359 | 366 | PF00069 | 0.550 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.541 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.391 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.447 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.531 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.588 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.724 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.547 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.458 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.753 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.420 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.536 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.837 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.668 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.395 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.348 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.384 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.423 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.756 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.583 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.708 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.605 |
MOD_GlcNHglycan | 369 | 373 | PF01048 | 0.505 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.690 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.465 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.714 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.484 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.697 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.518 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.508 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.592 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.586 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.540 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.783 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.725 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.397 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.480 |
MOD_N-GLC_1 | 632 | 637 | PF02516 | 0.412 |
MOD_N-GLC_1 | 648 | 653 | PF02516 | 0.336 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.814 |
MOD_N-GLC_2 | 696 | 698 | PF02516 | 0.545 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.511 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.375 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.690 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.353 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.349 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.443 |
MOD_NEK2_2 | 188 | 193 | PF00069 | 0.579 |
MOD_NEK2_2 | 255 | 260 | PF00069 | 0.540 |
MOD_NEK2_2 | 522 | 527 | PF00069 | 0.348 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.678 |
MOD_PIKK_1 | 196 | 202 | PF00454 | 0.498 |
MOD_PIKK_1 | 468 | 474 | PF00454 | 0.395 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.806 |
MOD_PK_1 | 714 | 720 | PF00069 | 0.482 |
MOD_PKA_1 | 706 | 712 | PF00069 | 0.617 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.364 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.443 |
MOD_PKA_2 | 706 | 712 | PF00069 | 0.609 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.488 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.481 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.550 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.534 |
MOD_Plk_1 | 468 | 474 | PF00069 | 0.348 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.348 |
MOD_Plk_1 | 648 | 654 | PF00069 | 0.443 |
MOD_Plk_2-3 | 298 | 304 | PF00069 | 0.580 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.471 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.451 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.435 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.556 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.694 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.356 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.348 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.361 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.408 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.756 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.573 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.702 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.547 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.748 |
MOD_ProDKin_1 | 650 | 656 | PF00069 | 0.348 |
MOD_SUMO_rev_2 | 643 | 648 | PF00179 | 0.475 |
TRG_DiLeu_BaEn_1 | 559 | 564 | PF01217 | 0.497 |
TRG_DiLeu_BaEn_2 | 220 | 226 | PF01217 | 0.472 |
TRG_DiLeu_BaLyEn_6 | 558 | 563 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.248 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 475 | 478 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 550 | 553 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.558 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 445 | 447 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 705 | 707 | PF00400 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 279 | 283 | PF00026 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 530 | 534 | PF00026 | 0.348 |
TRG_Pf-PMV_PEXEL_1 | 561 | 566 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Y4 | Leptomonas seymouri | 68% | 100% |
A0A0S4IPG9 | Bodo saltans | 43% | 97% |
A0A0S4IRJ2 | Bodo saltans | 46% | 100% |
A0A1X0P936 | Trypanosomatidae | 54% | 100% |
A0A3R7KV25 | Trypanosoma rangeli | 55% | 100% |
A0A3S7X2R6 | Leishmania donovani | 100% | 100% |
A4HHP3 | Leishmania braziliensis | 82% | 100% |
C9ZL03 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AEA6 | Leishmania major | 94% | 100% |
E9ALI0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5DTU5 | Trypanosoma cruzi | 54% | 100% |