A large and apprently artificial collection of diverse kinetoplastid protein kinases. A subfamily has 2TM regions, but the majority is cytoplasmic.
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HJS4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0007059 | chromosome segregation | 2 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 21 | 25 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 602 | 606 | PF00656 | 0.188 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.657 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.555 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 17 | 19 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 255 | 257 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 453 | 455 | PF00082 | 0.294 |
CLV_PCSK_PC7_1 | 208 | 214 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.277 |
DEG_APCC_DBOX_1 | 356 | 364 | PF00400 | 0.328 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.749 |
DOC_ANK_TNKS_1 | 576 | 583 | PF00023 | 0.294 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.741 |
DOC_CYCLIN_RxL_1 | 240 | 251 | PF00134 | 0.424 |
DOC_CYCLIN_yCln2_LP_2 | 480 | 486 | PF00134 | 0.414 |
DOC_CYCLIN_yCln2_LP_2 | 666 | 669 | PF00134 | 0.668 |
DOC_MAPK_gen_1 | 170 | 177 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 241 | 249 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 241 | 249 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 431 | 439 | PF00069 | 0.414 |
DOC_PP1_RVXF_1 | 462 | 468 | PF00149 | 0.414 |
DOC_PP1_RVXF_1 | 597 | 604 | PF00149 | 0.328 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.553 |
DOC_PP2B_LxvP_1 | 666 | 669 | PF13499 | 0.675 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.676 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.294 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.685 |
DOC_USP7_UBL2_3 | 329 | 333 | PF12436 | 0.428 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.414 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 661 | 666 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.711 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 241 | 246 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 303 | 310 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 454 | 459 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 475 | 481 | PF00244 | 0.404 |
LIG_Actin_WH2_2 | 307 | 322 | PF00022 | 0.550 |
LIG_APCC_ABBA_1 | 494 | 499 | PF00400 | 0.414 |
LIG_BIR_III_2 | 24 | 28 | PF00653 | 0.522 |
LIG_BIR_III_2 | 672 | 676 | PF00653 | 0.680 |
LIG_BRCT_BRCA1_1 | 116 | 120 | PF00533 | 0.585 |
LIG_deltaCOP1_diTrp_1 | 371 | 376 | PF00928 | 0.294 |
LIG_deltaCOP1_diTrp_1 | 561 | 569 | PF00928 | 0.294 |
LIG_eIF4E_1 | 358 | 364 | PF01652 | 0.294 |
LIG_EVH1_2 | 544 | 548 | PF00568 | 0.294 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.589 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.488 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.517 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.441 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.700 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.294 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.491 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.382 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.414 |
LIG_Integrin_RGD_1 | 431 | 433 | PF01839 | 0.414 |
LIG_LIR_Apic_2 | 539 | 545 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 190 | 200 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 244 | 252 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 343 | 352 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 356 | 364 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 423 | 430 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 433 | 442 | PF02991 | 0.294 |
LIG_LIR_LC3C_4 | 53 | 56 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.297 |
LIG_NRBOX | 359 | 365 | PF00104 | 0.328 |
LIG_Pex14_2 | 369 | 373 | PF04695 | 0.294 |
LIG_Rb_pABgroove_1 | 420 | 428 | PF01858 | 0.294 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.565 |
LIG_SH2_CRK | 570 | 574 | PF00017 | 0.294 |
LIG_SH2_GRB2like | 442 | 445 | PF00017 | 0.440 |
LIG_SH2_SRC | 542 | 545 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.110 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 639 | 642 | PF00017 | 0.397 |
LIG_SH3_3 | 601 | 607 | PF00018 | 0.294 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.646 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.691 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 410 | 415 | PF11976 | 0.328 |
LIG_SUMO_SIM_par_1 | 53 | 59 | PF11976 | 0.719 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.772 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.767 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.568 |
LIG_TRFH_1 | 487 | 491 | PF08558 | 0.294 |
LIG_TYR_ITIM | 568 | 573 | PF00017 | 0.294 |
LIG_UBA3_1 | 360 | 366 | PF00899 | 0.294 |
LIG_UBA3_1 | 503 | 507 | PF00899 | 0.414 |
LIG_WRC_WIRS_1 | 455 | 460 | PF05994 | 0.343 |
MOD_CDK_SPK_2 | 550 | 555 | PF00069 | 0.294 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.644 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.755 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.742 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.698 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.412 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.328 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.294 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.597 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.567 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.673 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.504 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.294 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.294 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.504 |
MOD_Cter_Amidation | 168 | 171 | PF01082 | 0.570 |
MOD_Cter_Amidation | 574 | 577 | PF01082 | 0.294 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.651 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.509 |
MOD_GlcNHglycan | 281 | 285 | PF01048 | 0.633 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.404 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.294 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.669 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.634 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.725 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.612 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.560 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.601 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.515 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.750 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.188 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.294 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.262 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.294 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.511 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.734 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.741 |
MOD_N-GLC_2 | 661 | 663 | PF02516 | 0.472 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.694 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.472 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.524 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.452 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.301 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.379 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.509 |
MOD_NEK2_2 | 266 | 271 | PF00069 | 0.312 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.525 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.232 |
MOD_PIKK_1 | 531 | 537 | PF00454 | 0.294 |
MOD_PIKK_1 | 581 | 587 | PF00454 | 0.294 |
MOD_PIKK_1 | 632 | 638 | PF00454 | 0.309 |
MOD_PKA_1 | 645 | 651 | PF00069 | 0.478 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.567 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.515 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.294 |
MOD_PKA_2 | 641 | 647 | PF00069 | 0.517 |
MOD_PKB_1 | 18 | 26 | PF00069 | 0.777 |
MOD_PKB_1 | 278 | 286 | PF00069 | 0.615 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.651 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.676 |
MOD_Plk_2-3 | 499 | 505 | PF00069 | 0.414 |
MOD_Plk_2-3 | 526 | 532 | PF00069 | 0.294 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.563 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.568 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.357 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.340 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.294 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.523 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.706 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.414 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.294 |
MOD_ProDKin_1 | 661 | 667 | PF00069 | 0.705 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.715 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.720 |
MOD_SUMO_for_1 | 143 | 146 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 313 | 319 | PF00179 | 0.460 |
MOD_SUMO_rev_2 | 323 | 331 | PF00179 | 0.392 |
MOD_SUMO_rev_2 | 482 | 492 | PF00179 | 0.397 |
MOD_SUMO_rev_2 | 499 | 509 | PF00179 | 0.194 |
MOD_SUMO_rev_2 | 610 | 616 | PF00179 | 0.294 |
TRG_DiLeu_BaEn_2 | 326 | 332 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_4 | 257 | 263 | PF01217 | 0.560 |
TRG_DiLeu_BaLyEn_6 | 461 | 466 | PF01217 | 0.309 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 455 | 458 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.289 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.525 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 586 | 588 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.769 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 586 | 590 | PF00026 | 0.328 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBJ1 | Leptomonas seymouri | 76% | 99% |
A0A1X0NJ50 | Trypanosomatidae | 58% | 100% |
A0A3S5IR34 | Trypanosoma rangeli | 58% | 100% |
A0A3S7X4W6 | Leishmania donovani | 92% | 100% |
A4H485 | Leishmania braziliensis | 24% | 93% |
A4I790 | Leishmania infantum | 92% | 100% |
C9ZMG9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
C9ZWL6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9B285 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
O55047 | Mus musculus | 38% | 94% |
Q08CW1 | Xenopus tropicalis | 38% | 97% |
Q1ECX4 | Danio rerio | 35% | 97% |
Q39238 | Arabidopsis thaliana | 40% | 98% |
Q4Q5X3 | Leishmania major | 92% | 100% |
Q86UE8 | Homo sapiens | 36% | 88% |
Q8C0V0 | Mus musculus | 37% | 88% |
Q90ZY6 | Danio rerio | 35% | 90% |
Q9UKI8 | Homo sapiens | 37% | 88% |
V5B7L8 | Trypanosoma cruzi | 59% | 100% |