Phosphatase, inositol-1,4,5-trisphosphate (IP3) 5-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 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HV10
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016311 | dephosphorylation | 5 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0019751 | polyol metabolic process | 4 | 1 |
GO:0019932 | second-messenger-mediated signaling | 4 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0043647 | inositol phosphate metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0046164 | alcohol catabolic process | 4 | 1 |
GO:0046174 | polyol catabolic process | 5 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046838 | obsolete phosphorylated carbohydrate dephosphorylation | 4 | 1 |
GO:0046855 | obsolete inositol phosphate dephosphorylation | 5 | 1 |
GO:0048016 | inositol phosphate-mediated signaling | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071545 | inositol phosphate catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 1 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0030258 | lipid modification | 4 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 1 |
GO:0046839 | phospholipid dephosphorylation | 5 | 1 |
GO:0046856 | phosphatidylinositol dephosphorylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004445 | inositol-polyphosphate 5-phosphatase activity | 8 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0016791 | phosphatase activity | 5 | 8 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 8 |
GO:0046030 | inositol trisphosphate phosphatase activity | 7 | 8 |
GO:0052658 | inositol-1,4,5-trisphosphate 5-phosphatase activity | 8 | 7 |
GO:0052659 | inositol-1,3,4,5-tetrakisphosphate 5-phosphatase activity | 8 | 7 |
GO:0052743 | inositol tetrakisphosphate phosphatase activity | 7 | 7 |
GO:0052745 | inositol phosphate phosphatase activity | 6 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.547 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.575 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.773 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.385 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 480 | 482 | PF00082 | 0.361 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 480 | 482 | PF00082 | 0.401 |
CLV_PCSK_PC7_1 | 453 | 459 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 406 | 410 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.413 |
DEG_APCC_DBOX_1 | 119 | 127 | PF00400 | 0.375 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.421 |
DEG_SCF_FBW7_1 | 578 | 584 | PF00400 | 0.533 |
DEG_SPOP_SBC_1 | 523 | 527 | PF00917 | 0.592 |
DOC_AGCK_PIF_3 | 685 | 688 | PF00069 | 0.390 |
DOC_CKS1_1 | 578 | 583 | PF01111 | 0.607 |
DOC_CYCLIN_yCln2_LP_2 | 421 | 427 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 359 | 369 | PF00069 | 0.528 |
DOC_MAPK_JIP1_4 | 33 | 39 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 182 | 190 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 361 | 369 | PF00069 | 0.470 |
DOC_MAPK_NFAT4_5 | 362 | 370 | PF00069 | 0.383 |
DOC_PP1_RVXF_1 | 615 | 621 | PF00149 | 0.319 |
DOC_PP2B_LxvP_1 | 324 | 327 | PF13499 | 0.460 |
DOC_PP2B_PxIxI_1 | 183 | 189 | PF00149 | 0.340 |
DOC_PP4_FxxP_1 | 312 | 315 | PF00568 | 0.392 |
DOC_PP4_FxxP_1 | 469 | 472 | PF00568 | 0.441 |
DOC_PP4_FxxP_1 | 86 | 89 | PF00568 | 0.589 |
DOC_SPAK_OSR1_1 | 20 | 24 | PF12202 | 0.542 |
DOC_SPAK_OSR1_1 | 481 | 485 | PF12202 | 0.411 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.618 |
DOC_USP7_UBL2_3 | 199 | 203 | PF12436 | 0.465 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 597 | 602 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.733 |
LIG_14-3-3_CanoR_1 | 125 | 129 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 20 | 24 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 247 | 253 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 575 | 581 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 632 | 637 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 662 | 671 | PF00244 | 0.475 |
LIG_APCC_ABBA_1 | 381 | 386 | PF00400 | 0.381 |
LIG_APCC_ABBA_1 | 425 | 430 | PF00400 | 0.307 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.325 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.418 |
LIG_BRCT_BRCA1_1 | 75 | 79 | PF00533 | 0.616 |
LIG_deltaCOP1_diTrp_1 | 463 | 469 | PF00928 | 0.381 |
LIG_eIF4E_1 | 671 | 677 | PF01652 | 0.327 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.515 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.523 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.493 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.598 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.646 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.369 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.623 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.443 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.629 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.652 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.374 |
LIG_GSK3_LRP6_1 | 157 | 162 | PF00069 | 0.628 |
LIG_LIR_Apic_2 | 309 | 315 | PF02991 | 0.388 |
LIG_LIR_Apic_2 | 467 | 472 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 84 | 89 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 301 | 312 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 463 | 473 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 511 | 517 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 682 | 688 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 76 | 86 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 90 | 98 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 511 | 515 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 666 | 671 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 682 | 688 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 90 | 94 | PF02991 | 0.495 |
LIG_Pex14_2 | 205 | 209 | PF04695 | 0.425 |
LIG_Pex14_2 | 21 | 25 | PF04695 | 0.606 |
LIG_Pex14_2 | 465 | 469 | PF04695 | 0.410 |
LIG_PTB_Apo_2 | 199 | 206 | PF02174 | 0.458 |
LIG_Rb_LxCxE_1 | 455 | 477 | PF01857 | 0.450 |
LIG_SH2_CRK | 512 | 516 | PF00017 | 0.467 |
LIG_SH2_NCK_1 | 512 | 516 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 671 | 675 | PF00017 | 0.400 |
LIG_SH2_PTP2 | 331 | 334 | PF00017 | 0.432 |
LIG_SH2_PTP2 | 91 | 94 | PF00017 | 0.583 |
LIG_SH2_SRC | 331 | 334 | PF00017 | 0.432 |
LIG_SH2_SRC | 669 | 672 | PF00017 | 0.391 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 512 | 516 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 669 | 673 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 400 | 403 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.583 |
LIG_SH3_1 | 634 | 640 | PF00018 | 0.621 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.595 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.490 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.613 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.500 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.655 |
LIG_SH3_3 | 634 | 640 | PF00018 | 0.634 |
LIG_SUMO_SIM_anti_2 | 187 | 192 | PF11976 | 0.293 |
LIG_SUMO_SIM_anti_2 | 35 | 40 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 491 | 498 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 35 | 40 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 416 | 423 | PF11976 | 0.409 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.418 |
LIG_WRC_WIRS_1 | 82 | 87 | PF05994 | 0.479 |
LIG_WW_2 | 6 | 9 | PF00397 | 0.612 |
MOD_CDC14_SPxK_1 | 600 | 603 | PF00782 | 0.496 |
MOD_CDK_SPK_2 | 311 | 316 | PF00069 | 0.396 |
MOD_CDK_SPxK_1 | 597 | 603 | PF00069 | 0.496 |
MOD_CDK_SPxxK_3 | 102 | 109 | PF00069 | 0.594 |
MOD_CDK_SPxxK_3 | 175 | 182 | PF00069 | 0.516 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.431 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.630 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.683 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.697 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.656 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.423 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.369 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.447 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.640 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.615 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.654 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.499 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.534 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.658 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.355 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.476 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.394 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.646 |
MOD_Cter_Amidation | 401 | 404 | PF01082 | 0.404 |
MOD_DYRK1A_RPxSP_1 | 175 | 179 | PF00069 | 0.501 |
MOD_DYRK1A_RPxSP_1 | 63 | 67 | PF00069 | 0.598 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.555 |
MOD_GlcNHglycan | 137 | 141 | PF01048 | 0.531 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.540 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.573 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.619 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.428 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.609 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.643 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.384 |
MOD_GlcNHglycan | 414 | 418 | PF01048 | 0.415 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.616 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.661 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.468 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.610 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.555 |
MOD_GlcNHglycan | 74 | 78 | PF01048 | 0.686 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.498 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.529 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.518 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.667 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.437 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.787 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.701 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.397 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.450 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.605 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.636 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.531 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.457 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.605 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.734 |
MOD_N-GLC_1 | 13 | 18 | PF02516 | 0.503 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.693 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.630 |
MOD_N-GLC_2 | 377 | 379 | PF02516 | 0.368 |
MOD_N-GLC_2 | 605 | 607 | PF02516 | 0.450 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.721 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.486 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.421 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.321 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.406 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.474 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.636 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.665 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.335 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.604 |
MOD_PKA_1 | 256 | 262 | PF00069 | 0.657 |
MOD_PKA_2 | 124 | 130 | PF00069 | 0.408 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.536 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.427 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.455 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.614 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.675 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.600 |
MOD_PKB_1 | 245 | 253 | PF00069 | 0.612 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.418 |
MOD_Plk_2-3 | 436 | 442 | PF00069 | 0.349 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.408 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.449 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.326 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.446 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.469 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.658 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.596 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.698 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.521 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.630 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.432 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.386 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.654 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.624 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.641 |
MOD_ProDKin_1 | 597 | 603 | PF00069 | 0.496 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.727 |
MOD_SUMO_rev_2 | 26 | 35 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 430 | 440 | PF00179 | 0.384 |
MOD_SUMO_rev_2 | 442 | 448 | PF00179 | 0.449 |
TRG_DiLeu_BaEn_1 | 485 | 490 | PF01217 | 0.358 |
TRG_DiLeu_BaLyEn_6 | 181 | 186 | PF01217 | 0.445 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 671 | 674 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.583 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 403 | 406 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 478 | 481 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 517 | 520 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 572 | 575 | PF00400 | 0.670 |
TRG_NLS_MonoExtN_4 | 456 | 461 | PF00514 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 406 | 410 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E4 | Leptomonas seymouri | 51% | 100% |
A0A3S5H6J4 | Leishmania donovani | 100% | 100% |
A0A422NRL6 | Trypanosoma rangeli | 30% | 100% |
A4H6M7 | Leishmania braziliensis | 75% | 100% |
E9ANP5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
Q4QGX8 | Leishmania major | 93% | 100% |