Glycosome membrane, Peroxin 6 peroxisome assembly
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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005778 | peroxisomal membrane | 6 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0031903 | microbody membrane | 5 | 1 |
GO:0042579 | microbody | 5 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HWQ5
Term | Name | Level | Count |
---|---|---|---|
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0042254 | ribosome biogenesis | 5 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0044085 | cellular component biogenesis | 3 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051052 | regulation of DNA metabolic process | 5 | 1 |
GO:0051054 | positive regulation of DNA metabolic process | 6 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 1 |
GO:0051972 | regulation of telomerase activity | 5 | 1 |
GO:0051973 | positive regulation of telomerase activity | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:2000278 | regulation of DNA biosynthetic process | 6 | 1 |
GO:2000573 | positive regulation of DNA biosynthetic process | 7 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006625 | protein targeting to peroxisome | 5 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007031 | peroxisome organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0015919 | peroxisomal membrane transport | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016558 | protein import into peroxisome matrix | 5 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0043574 | peroxisomal transport | 4 | 1 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071806 | protein transmembrane transport | 3 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072662 | protein localization to peroxisome | 6 | 1 |
GO:0072663 | establishment of protein localization to peroxisome | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0016462 | pyrophosphatase activity | 5 | 15 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 15 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 15 |
GO:0016887 | ATP hydrolysis activity | 7 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 15 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:1990275 | preribosome binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.428 |
CLV_C14_Caspase3-7 | 665 | 669 | PF00656 | 0.304 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 756 | 758 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 834 | 836 | PF00675 | 0.631 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 701 | 703 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 575 | 577 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 598 | 600 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 701 | 703 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 648 | 652 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 674 | 678 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 836 | 840 | PF00082 | 0.386 |
DEG_APCC_DBOX_1 | 380 | 388 | PF00400 | 0.355 |
DEG_APCC_KENBOX_2 | 343 | 347 | PF00400 | 0.380 |
DEG_SCF_FBW7_1 | 79 | 86 | PF00400 | 0.484 |
DEG_SCF_FBW7_2 | 326 | 332 | PF00400 | 0.453 |
DOC_CDC14_PxL_1 | 581 | 589 | PF14671 | 0.490 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.447 |
DOC_CKS1_1 | 46 | 51 | PF01111 | 0.484 |
DOC_CKS1_1 | 5 | 10 | PF01111 | 0.488 |
DOC_CYCLIN_yCln2_LP_2 | 128 | 134 | PF00134 | 0.416 |
DOC_CYCLIN_yCln2_LP_2 | 722 | 728 | PF00134 | 0.326 |
DOC_MAPK_gen_1 | 260 | 270 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 575 | 586 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 594 | 604 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 732 | 741 | PF00069 | 0.317 |
DOC_MAPK_HePTP_8 | 683 | 695 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 251 | 258 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 579 | 586 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 655 | 663 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 686 | 695 | PF00069 | 0.254 |
DOC_MAPK_MEF2A_6 | 835 | 842 | PF00069 | 0.257 |
DOC_MAPK_NFAT4_5 | 251 | 259 | PF00069 | 0.483 |
DOC_MAPK_NFAT4_5 | 579 | 587 | PF00069 | 0.356 |
DOC_PP1_RVXF_1 | 157 | 163 | PF00149 | 0.437 |
DOC_PP1_RVXF_1 | 431 | 437 | PF00149 | 0.324 |
DOC_PP1_RVXF_1 | 646 | 652 | PF00149 | 0.254 |
DOC_PP2B_LxvP_1 | 128 | 131 | PF13499 | 0.403 |
DOC_PP2B_LxvP_1 | 739 | 742 | PF13499 | 0.391 |
DOC_PP4_FxxP_1 | 359 | 362 | PF00568 | 0.497 |
DOC_PP4_FxxP_1 | 473 | 476 | PF00568 | 0.445 |
DOC_PP4_FxxP_1 | 604 | 607 | PF00568 | 0.254 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 785 | 789 | PF00917 | 0.300 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.543 |
DOC_USP7_MATH_2 | 137 | 143 | PF00917 | 0.435 |
DOC_USP7_UBL2_3 | 594 | 598 | PF12436 | 0.427 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.254 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 816 | 821 | PF00397 | 0.643 |
LIG_14-3-3_CanoR_1 | 197 | 206 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 230 | 239 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 41 | 49 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 421 | 425 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 486 | 492 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 686 | 695 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 835 | 841 | PF00244 | 0.433 |
LIG_Actin_WH2_2 | 839 | 855 | PF00022 | 0.303 |
LIG_BIR_III_2 | 443 | 447 | PF00653 | 0.362 |
LIG_BIR_III_4 | 679 | 683 | PF00653 | 0.254 |
LIG_BRCT_BRCA1_1 | 623 | 627 | PF00533 | 0.255 |
LIG_CaM_IQ_9 | 310 | 326 | PF13499 | 0.320 |
LIG_CaM_NSCaTE_8 | 194 | 201 | PF13499 | 0.633 |
LIG_Clathr_ClatBox_1 | 692 | 696 | PF01394 | 0.269 |
LIG_EVH1_1 | 4 | 8 | PF00568 | 0.535 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.591 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.565 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.510 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.581 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.449 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.429 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.614 |
LIG_FHA_1 | 598 | 604 | PF00498 | 0.423 |
LIG_FHA_1 | 806 | 812 | PF00498 | 0.627 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.387 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.766 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.478 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.562 |
LIG_FHA_2 | 452 | 458 | PF00498 | 0.539 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.462 |
LIG_FHA_2 | 742 | 748 | PF00498 | 0.362 |
LIG_FHA_2 | 777 | 783 | PF00498 | 0.308 |
LIG_FHA_2 | 855 | 861 | PF00498 | 0.349 |
LIG_GBD_Chelix_1 | 32 | 40 | PF00786 | 0.537 |
LIG_KLC1_Yacidic_2 | 203 | 208 | PF13176 | 0.493 |
LIG_LIR_Gen_1 | 506 | 514 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 550 | 560 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 624 | 635 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 506 | 510 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 550 | 556 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 624 | 630 | PF02991 | 0.221 |
LIG_LIR_Nem_3 | 782 | 786 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.402 |
LIG_LYPXL_yS_3 | 179 | 182 | PF13949 | 0.525 |
LIG_MYND_1 | 585 | 589 | PF01753 | 0.381 |
LIG_NRBOX | 51 | 57 | PF00104 | 0.394 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.338 |
LIG_SH2_CRK | 553 | 557 | PF00017 | 0.477 |
LIG_SH2_CRK | 605 | 609 | PF00017 | 0.304 |
LIG_SH2_GRB2like | 123 | 126 | PF00017 | 0.548 |
LIG_SH2_NCK_1 | 107 | 111 | PF00017 | 0.549 |
LIG_SH2_NCK_1 | 553 | 557 | PF00017 | 0.482 |
LIG_SH2_SRC | 507 | 510 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 123 | 127 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 507 | 511 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.703 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 738 | 741 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 778 | 781 | PF00017 | 0.312 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.482 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.549 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.480 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.510 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.632 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.254 |
LIG_SH3_3 | 767 | 773 | PF00018 | 0.458 |
LIG_SH3_CIN85_PxpxPR_1 | 428 | 433 | PF14604 | 0.403 |
LIG_SUMO_SIM_anti_2 | 220 | 227 | PF11976 | 0.654 |
LIG_SUMO_SIM_anti_2 | 284 | 289 | PF11976 | 0.581 |
LIG_SUMO_SIM_anti_2 | 391 | 397 | PF11976 | 0.322 |
LIG_SUMO_SIM_anti_2 | 509 | 515 | PF11976 | 0.347 |
LIG_SUMO_SIM_anti_2 | 530 | 537 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 509 | 515 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 691 | 696 | PF11976 | 0.269 |
LIG_TRAF2_1 | 370 | 373 | PF00917 | 0.455 |
LIG_TRAF2_1 | 465 | 468 | PF00917 | 0.484 |
LIG_TRAF2_1 | 744 | 747 | PF00917 | 0.370 |
LIG_TRAF2_1 | 798 | 801 | PF00917 | 0.519 |
LIG_TRAF2_1 | 830 | 833 | PF00917 | 0.709 |
LIG_TYR_ITIM | 177 | 182 | PF00017 | 0.548 |
LIG_TYR_ITIM | 505 | 510 | PF00017 | 0.443 |
LIG_TYR_ITIM | 736 | 741 | PF00017 | 0.304 |
LIG_UBA3_1 | 749 | 753 | PF00899 | 0.373 |
LIG_WRC_WIRS_1 | 335 | 340 | PF05994 | 0.423 |
MOD_CDK_SPK_2 | 491 | 496 | PF00069 | 0.486 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.509 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.480 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.370 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.450 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.526 |
MOD_CK1_1 | 703 | 709 | PF00069 | 0.292 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.491 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.663 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.517 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.414 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.370 |
MOD_DYRK1A_RPxSP_1 | 325 | 329 | PF00069 | 0.394 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.698 |
MOD_GlcNHglycan | 139 | 144 | PF01048 | 0.508 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.511 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.596 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.410 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.553 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.427 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.375 |
MOD_GlcNHglycan | 760 | 764 | PF01048 | 0.376 |
MOD_GlcNHglycan | 766 | 770 | PF01048 | 0.340 |
MOD_GlcNHglycan | 821 | 824 | PF01048 | 0.655 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.486 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.511 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.578 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.468 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.454 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.362 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.380 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.485 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.518 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.565 |
MOD_GSK3_1 | 867 | 874 | PF00069 | 0.491 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.494 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.466 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.650 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.566 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.691 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.459 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.439 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.472 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.451 |
MOD_NEK2_1 | 776 | 781 | PF00069 | 0.321 |
MOD_NEK2_1 | 811 | 816 | PF00069 | 0.626 |
MOD_NEK2_1 | 871 | 876 | PF00069 | 0.483 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.593 |
MOD_PIKK_1 | 686 | 692 | PF00454 | 0.386 |
MOD_PKA_1 | 597 | 603 | PF00069 | 0.424 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.581 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.587 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.539 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.620 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.525 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.458 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.387 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.594 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.456 |
MOD_Plk_1 | 621 | 627 | PF00069 | 0.234 |
MOD_Plk_1 | 765 | 771 | PF00069 | 0.472 |
MOD_Plk_2-3 | 279 | 285 | PF00069 | 0.469 |
MOD_Plk_2-3 | 509 | 515 | PF00069 | 0.420 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.451 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.628 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.426 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.498 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.530 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.413 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.333 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.368 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.515 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.304 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.756 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.500 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.585 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.578 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.481 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.535 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.254 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.476 |
MOD_ProDKin_1 | 816 | 822 | PF00069 | 0.645 |
MOD_SUMO_for_1 | 574 | 577 | PF00179 | 0.350 |
MOD_SUMO_rev_2 | 832 | 838 | PF00179 | 0.590 |
TRG_DiLeu_BaEn_2 | 771 | 777 | PF01217 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 473 | 478 | PF01217 | 0.473 |
TRG_DiLeu_BaLyEn_6 | 645 | 650 | PF01217 | 0.254 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 507 | 510 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 738 | 741 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 864 | 867 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 846 | 849 | PF00400 | 0.284 |
TRG_NES_CRM1_1 | 577 | 590 | PF08389 | 0.502 |
TRG_NLS_MonoExtN_4 | 594 | 601 | PF00514 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 576 | 580 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 648 | 652 | PF00026 | 0.254 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7Z4 | Leptomonas seymouri | 68% | 90% |
A0A1X0NZ72 | Trypanosomatidae | 41% | 92% |
A0A3S5H6W4 | Leishmania donovani | 99% | 91% |
A0A3S7X0L3 | Leishmania donovani | 36% | 100% |
A0A422NAC8 | Trypanosoma rangeli | 47% | 100% |
A4H8D3 | Leishmania braziliensis | 81% | 100% |
A4I2Q7 | Leishmania infantum | 36% | 100% |
C9ZPS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 89% |
E9AD83 | Leishmania major | 35% | 100% |
E9AQG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AZ07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
Q4QF14 | Leishmania major | 94% | 100% |
V5ARC8 | Trypanosoma cruzi | 44% | 92% |