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: 20 |
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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 12 |
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: O97198
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006811 | monoatomic ion transport | 4 | 12 |
GO:0006812 | monoatomic cation transport | 5 | 12 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 4 |
GO:0006885 | regulation of pH | 8 | 4 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019725 | cellular homeostasis | 2 | 4 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 4 |
GO:0030004 | obsolete cellular monovalent inorganic cation homeostasis | 6 | 4 |
GO:0030641 | regulation of cellular pH | 7 | 4 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 12 |
GO:0042592 | homeostatic process | 3 | 4 |
GO:0048878 | chemical homeostasis | 4 | 4 |
GO:0050801 | monoatomic ion homeostasis | 5 | 4 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051453 | regulation of intracellular pH | 8 | 4 |
GO:0055067 | obsolete monovalent inorganic cation homeostasis | 7 | 4 |
GO:0055080 | monoatomic cation homeostasis | 6 | 4 |
GO:0055082 | intracellular chemical homeostasis | 3 | 4 |
GO:0055085 | transmembrane transport | 2 | 12 |
GO:0065007 | biological regulation | 1 | 4 |
GO:0065008 | regulation of biological quality | 2 | 4 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 12 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 12 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 12 |
GO:0098771 | inorganic ion homeostasis | 6 | 4 |
GO:1902600 | proton transmembrane transport | 6 | 12 |
GO:0120029 | proton export across plasma membrane | 4 | 10 |
GO:0140115 | export across plasma membrane | 3 | 10 |
GO:0140352 | export from cell | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0005215 | transporter activity | 1 | 12 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 12 |
GO:0008553 | P-type proton-exporting transporter activity | 4 | 12 |
GO:0009678 | pyrophosphate hydrolysis-driven proton transmembrane transporter activity | 5 | 12 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 12 |
GO:0015078 | proton transmembrane transporter activity | 5 | 12 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 12 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 12 |
GO:0015662 | P-type ion transporter activity | 4 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 16 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 16 |
GO:0016887 | ATP hydrolysis activity | 7 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 16 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 12 |
GO:0022804 | active transmembrane transporter activity | 3 | 12 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 12 |
GO:0022857 | transmembrane transporter activity | 2 | 12 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140358 | P-type transmembrane transporter activity | 3 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 923 | 927 | PF00656 | 0.517 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 768 | 770 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 819 | 821 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 904 | 906 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 917 | 919 | PF00675 | 0.368 |
CLV_PCSK_FUR_1 | 115 | 119 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 768 | 770 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 819 | 821 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 904 | 906 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 917 | 919 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.247 |
CLV_PCSK_PC7_1 | 113 | 119 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 738 | 742 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 824 | 828 | PF00082 | 0.332 |
DEG_APCC_DBOX_1 | 425 | 433 | PF00400 | 0.464 |
DEG_APCC_DBOX_1 | 819 | 827 | PF00400 | 0.574 |
DEG_MDM2_SWIB_1 | 92 | 99 | PF02201 | 0.184 |
DOC_ANK_TNKS_1 | 120 | 127 | PF00023 | 0.467 |
DOC_ANK_TNKS_1 | 881 | 888 | PF00023 | 0.623 |
DOC_CDC14_PxL_1 | 281 | 289 | PF14671 | 0.356 |
DOC_CKS1_1 | 15 | 20 | PF01111 | 0.502 |
DOC_CKS1_1 | 947 | 952 | PF01111 | 0.579 |
DOC_CYCLIN_RxL_1 | 312 | 322 | PF00134 | 0.425 |
DOC_CYCLIN_RxL_1 | 647 | 655 | PF00134 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 282 | 288 | PF00134 | 0.394 |
DOC_MAPK_gen_1 | 271 | 281 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 313 | 320 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 411 | 420 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 424 | 431 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 816 | 825 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 306 | 314 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 495 | 502 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 605 | 613 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 819 | 827 | PF00069 | 0.530 |
DOC_MAPK_NFAT4_5 | 824 | 832 | PF00069 | 0.393 |
DOC_PP1_RVXF_1 | 444 | 450 | PF00149 | 0.454 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.356 |
DOC_PP2B_LxvP_1 | 695 | 698 | PF13499 | 0.421 |
DOC_PP4_FxxP_1 | 478 | 481 | PF00568 | 0.500 |
DOC_SPAK_OSR1_1 | 60 | 64 | PF12202 | 0.356 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 921 | 925 | PF00917 | 0.539 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 773 | 778 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 806 | 811 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 906 | 911 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 946 | 951 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 237 | 246 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 315 | 321 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 541 | 551 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 605 | 613 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 904 | 910 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 917 | 925 | PF00244 | 0.535 |
LIG_AP2alpha_2 | 468 | 470 | PF02296 | 0.444 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.682 |
LIG_BIR_III_2 | 485 | 489 | PF00653 | 0.446 |
LIG_BIR_III_2 | 842 | 846 | PF00653 | 0.314 |
LIG_BIR_III_4 | 913 | 917 | PF00653 | 0.587 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.394 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.371 |
LIG_BRCT_BRCA1_1 | 657 | 661 | PF00533 | 0.524 |
LIG_EH1_1 | 60 | 68 | PF00400 | 0.356 |
LIG_eIF4E_1 | 165 | 171 | PF01652 | 0.490 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.399 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.534 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.479 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.447 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.453 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.401 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.468 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.472 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.629 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.353 |
LIG_FHA_1 | 791 | 797 | PF00498 | 0.353 |
LIG_FHA_1 | 836 | 842 | PF00498 | 0.430 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.545 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.490 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.471 |
LIG_FHA_2 | 475 | 481 | PF00498 | 0.496 |
LIG_GBD_Chelix_1 | 756 | 764 | PF00786 | 0.454 |
LIG_LIR_Apic_2 | 477 | 481 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 133 | 144 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 390 | 398 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 651 | 661 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 93 | 104 | PF02991 | 0.348 |
LIG_LIR_LC3C_4 | 644 | 648 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 19 | 24 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 651 | 656 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 658 | 663 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 724 | 730 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 746 | 752 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 793 | 798 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.348 |
LIG_MLH1_MIPbox_1 | 240 | 244 | PF16413 | 0.356 |
LIG_MLH1_MIPbox_1 | 657 | 661 | PF16413 | 0.490 |
LIG_NRBOX | 277 | 283 | PF00104 | 0.394 |
LIG_NRBOX | 313 | 319 | PF00104 | 0.526 |
LIG_NRBOX | 471 | 477 | PF00104 | 0.430 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.184 |
LIG_RPA_C_Fungi | 408 | 420 | PF08784 | 0.259 |
LIG_SH2_CRK | 854 | 858 | PF00017 | 0.300 |
LIG_SH2_GRB2like | 709 | 712 | PF00017 | 0.446 |
LIG_SH2_GRB2like | 798 | 801 | PF00017 | 0.218 |
LIG_SH2_NCK_1 | 81 | 85 | PF00017 | 0.289 |
LIG_SH2_PTP2 | 293 | 296 | PF00017 | 0.205 |
LIG_SH2_SRC | 397 | 400 | PF00017 | 0.475 |
LIG_SH2_SRC | 709 | 712 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 657 | 661 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 709 | 712 | PF00017 | 0.218 |
LIG_SH2_STAT5 | 795 | 798 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 854 | 857 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 874 | 877 | PF00017 | 0.273 |
LIG_SH3_1 | 944 | 950 | PF00018 | 0.454 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.547 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.456 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.335 |
LIG_SH3_3 | 676 | 682 | PF00018 | 0.218 |
LIG_SH3_3 | 897 | 903 | PF00018 | 0.570 |
LIG_SH3_3 | 944 | 950 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 218 | 223 | PF11976 | 0.463 |
LIG_SUMO_SIM_anti_2 | 275 | 283 | PF11976 | 0.243 |
LIG_SUMO_SIM_anti_2 | 427 | 433 | PF11976 | 0.449 |
LIG_SUMO_SIM_anti_2 | 499 | 504 | PF11976 | 0.237 |
LIG_SUMO_SIM_anti_2 | 644 | 649 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 217 | 223 | PF11976 | 0.218 |
LIG_SUMO_SIM_par_1 | 316 | 322 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 324 | 329 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 548 | 554 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 644 | 649 | PF11976 | 0.385 |
LIG_TYR_ITIM | 796 | 801 | PF00017 | 0.245 |
LIG_Vh1_VBS_1 | 663 | 681 | PF01044 | 0.165 |
LIG_WRC_WIRS_1 | 475 | 480 | PF05994 | 0.334 |
LIG_WRC_WIRS_1 | 791 | 796 | PF05994 | 0.218 |
LIG_WW_3 | 29 | 33 | PF00397 | 0.391 |
MOD_CDC14_SPxK_1 | 809 | 812 | PF00782 | 0.536 |
MOD_CDK_SPxK_1 | 806 | 812 | PF00069 | 0.517 |
MOD_CDK_SPxxK_3 | 53 | 60 | PF00069 | 0.312 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.487 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.355 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.242 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.442 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.338 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.452 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.570 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.353 |
MOD_CK1_1 | 806 | 812 | PF00069 | 0.456 |
MOD_CK1_1 | 908 | 914 | PF00069 | 0.523 |
MOD_CK1_1 | 919 | 925 | PF00069 | 0.405 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.392 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.430 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.288 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.358 |
MOD_CK2_1 | 686 | 692 | PF00069 | 0.443 |
MOD_CK2_1 | 946 | 952 | PF00069 | 0.728 |
MOD_CMANNOS | 815 | 818 | PF00535 | 0.401 |
MOD_Cter_Amidation | 915 | 918 | PF01082 | 0.487 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.336 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.275 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.321 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.446 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.471 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.323 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.573 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.404 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.547 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.317 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.459 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.470 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.457 |
MOD_GlcNHglycan | 552 | 556 | PF01048 | 0.555 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.325 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.454 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.411 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.500 |
MOD_GlcNHglycan | 919 | 922 | PF01048 | 0.429 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.285 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.435 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.278 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.278 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.320 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.326 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.359 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.505 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.331 |
MOD_GSK3_1 | 904 | 911 | PF00069 | 0.697 |
MOD_GSK3_1 | 916 | 923 | PF00069 | 0.440 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.343 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.315 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.296 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.314 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.315 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.310 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.439 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.438 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.410 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.353 |
MOD_NEK2_1 | 801 | 806 | PF00069 | 0.295 |
MOD_NEK2_1 | 835 | 840 | PF00069 | 0.274 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.552 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.218 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.424 |
MOD_NEK2_2 | 790 | 795 | PF00069 | 0.218 |
MOD_NEK2_2 | 865 | 870 | PF00069 | 0.337 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.428 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.315 |
MOD_PIKK_1 | 449 | 455 | PF00454 | 0.391 |
MOD_PK_1 | 424 | 430 | PF00069 | 0.313 |
MOD_PKA_1 | 904 | 910 | PF00069 | 0.517 |
MOD_PKA_1 | 917 | 923 | PF00069 | 0.431 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.353 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.218 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.259 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.421 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.424 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.350 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.304 |
MOD_PKA_2 | 818 | 824 | PF00069 | 0.543 |
MOD_PKA_2 | 903 | 909 | PF00069 | 0.770 |
MOD_PKA_2 | 916 | 922 | PF00069 | 0.445 |
MOD_PKB_1 | 367 | 375 | PF00069 | 0.324 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.218 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.281 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.357 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.526 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.447 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.512 |
MOD_Plk_1 | 498 | 504 | PF00069 | 0.245 |
MOD_Plk_1 | 723 | 729 | PF00069 | 0.354 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.323 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.536 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.299 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.244 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.218 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.179 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.275 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.441 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.372 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.260 |
MOD_Plk_4 | 703 | 709 | PF00069 | 0.420 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.343 |
MOD_Plk_4 | 723 | 729 | PF00069 | 0.459 |
MOD_Plk_4 | 775 | 781 | PF00069 | 0.498 |
MOD_Plk_4 | 790 | 796 | PF00069 | 0.279 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.642 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.407 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.468 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.276 |
MOD_ProDKin_1 | 773 | 779 | PF00069 | 0.512 |
MOD_ProDKin_1 | 806 | 812 | PF00069 | 0.545 |
MOD_ProDKin_1 | 906 | 912 | PF00069 | 0.709 |
MOD_ProDKin_1 | 946 | 952 | PF00069 | 0.614 |
MOD_SUMO_for_1 | 520 | 523 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 934 | 940 | PF00179 | 0.429 |
TRG_DiLeu_BaEn_1 | 443 | 448 | PF01217 | 0.287 |
TRG_DiLeu_BaEn_3 | 133 | 139 | PF01217 | 0.205 |
TRG_DiLeu_BaEn_4 | 230 | 236 | PF01217 | 0.205 |
TRG_DiLeu_BaLyEn_6 | 282 | 287 | PF01217 | 0.165 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 727 | 730 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 798 | 801 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 854 | 857 | PF00928 | 0.268 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 232 | 235 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 312 | 315 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 43 | 46 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 682 | 684 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 818 | 820 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 822 | 825 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 903 | 905 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 942 | 945 | PF00400 | 0.467 |
TRG_NES_CRM1_1 | 637 | 651 | PF08389 | 0.263 |
TRG_Pf-PMV_PEXEL_1 | 582 | 586 | PF00026 | 0.287 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1X4 | Leptomonas seymouri | 42% | 94% |
A0A0S4JRV4 | Bodo saltans | 22% | 94% |
A0A1X0NL00 | Trypanosomatidae | 28% | 100% |
A0A1X0P0Y8 | Trypanosomatidae | 22% | 87% |
A0A1X0P720 | Trypanosomatidae | 29% | 100% |
A0A1X0P724 | Trypanosomatidae | 28% | 100% |
A0A1X0P7A1 | Trypanosomatidae | 28% | 99% |
A0A1X0P842 | Trypanosomatidae | 27% | 94% |
A0A381MFJ0 | Leishmania infantum | 26% | 98% |
A0A3S5H5E7 | Leishmania donovani | 93% | 99% |
A0A3S5IRL5 | Trypanosoma rangeli | 27% | 100% |
A0A3S7WV61 | Leishmania donovani | 26% | 98% |
A0A3S7WV68 | Leishmania donovani | 26% | 98% |
A4H9Q5 | Leishmania braziliensis | 28% | 100% |
A4HSA9 | Leishmania infantum | 93% | 99% |
A4HY23 | Leishmania infantum | 26% | 98% |
A7L9Z8 | Mus musculus | 22% | 100% |
E9AK92 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9ART6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 98% |
O14072 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 20% | 79% |
O59868 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
P05030 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P07038 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 100% |
P09627 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
P11718 | Leishmania donovani | 26% | 98% |
P12522 | Leishmania donovani | 26% | 98% |
P13586 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
P19657 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
P22036 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 26% | 100% |
P24545 | Zygosaccharomyces rouxii | 25% | 100% |
P28877 | Candida albicans | 27% | 100% |
P37367 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 24% | 100% |
P49380 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 25% | 100% |
P54678 | Dictyostelium discoideum | 20% | 85% |
P54679 | Dictyostelium discoideum | 25% | 90% |
P57709 | Bos taurus | 23% | 100% |
P63688 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 27% | 100% |
P98194 | Homo sapiens | 23% | 100% |
P9WPS8 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 27% | 100% |
P9WPS9 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 27% | 100% |
Q37145 | Arabidopsis thaliana | 21% | 93% |
Q4QDN7 | Leishmania major | 29% | 100% |
Q4QDN8 | Leishmania major | 29% | 100% |
Q5R5K5 | Pongo abelii | 23% | 100% |
Q64566 | Rattus norvegicus | 23% | 100% |
Q65X71 | Oryza sativa subsp. japonica | 21% | 93% |
Q73E41 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 22% | 100% |
Q8PCM1 | Xanthomonas campestris pv. campestris (strain ATCC 33913 / DSM 3586 / NCPPB 528 / LMG 568 / P 25) | 25% | 100% |
Q8PPC9 | Xanthomonas axonopodis pv. citri (strain 306) | 26% | 100% |
Q8R4C1 | Rattus norvegicus | 22% | 100% |
Q8Y8Q5 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 22% | 100% |
Q98GX6 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 24% | 100% |
Q9M2L4 | Arabidopsis thaliana | 22% | 93% |
Q9SZR1 | Arabidopsis thaliana | 23% | 89% |
Q9X8Z9 | Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) | 24% | 100% |