A large and apprently artificial collection of diverse kinetoplastid protein kinases. None of them appear to be TM.
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000922 | spindle pole | 2 | 2 |
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005813 | centrosome | 3 | 2 |
GO:0005815 | microtubule organizing center | 2 | 2 |
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 |
Related structures:
AlphaFold database: Q4QEC3
Term | Name | Level | Count |
---|---|---|---|
GO:0000278 | mitotic cell cycle | 3 | 2 |
GO:0006468 | protein phosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0007049 | cell cycle | 2 | 2 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010564 | regulation of cell cycle process | 5 | 2 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0032465 | regulation of cytokinesis | 5 | 2 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051302 | regulation of cell division | 4 | 2 |
GO:0051726 | regulation of cell cycle | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 10 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 478 | 482 | PF00656 | 0.543 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.259 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 621 | 623 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 666 | 668 | PF00082 | 0.261 |
CLV_PCSK_PC1ET2_1 | 201 | 203 | PF00082 | 0.237 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 621 | 623 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.237 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.179 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.204 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.366 |
CLV_Separin_Metazoa | 373 | 377 | PF03568 | 0.647 |
DEG_APCC_DBOX_1 | 287 | 295 | PF00400 | 0.255 |
DEG_APCC_DBOX_1 | 371 | 379 | PF00400 | 0.587 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.672 |
DEG_SCF_FBW7_1 | 306 | 313 | PF00400 | 0.498 |
DEG_SPOP_SBC_1 | 20 | 24 | PF00917 | 0.542 |
DEG_SPOP_SBC_1 | 327 | 331 | PF00917 | 0.710 |
DEG_SPOP_SBC_1 | 611 | 615 | PF00917 | 0.514 |
DOC_CKS1_1 | 307 | 312 | PF01111 | 0.542 |
DOC_CKS1_1 | 660 | 665 | PF01111 | 0.429 |
DOC_CYCLIN_yCln2_LP_2 | 308 | 314 | PF00134 | 0.548 |
DOC_MAPK_gen_1 | 100 | 110 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 115 | 124 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 168 | 177 | PF00069 | 0.315 |
DOC_MAPK_gen_1 | 621 | 632 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 666 | 672 | PF00069 | 0.499 |
DOC_PP1_RVXF_1 | 519 | 525 | PF00149 | 0.499 |
DOC_PP2B_LxvP_1 | 308 | 311 | PF13499 | 0.473 |
DOC_PP2B_LxvP_1 | 319 | 322 | PF13499 | 0.501 |
DOC_PP2B_LxvP_1 | 366 | 369 | PF13499 | 0.569 |
DOC_PP4_FxxP_1 | 317 | 320 | PF00568 | 0.601 |
DOC_SPAK_OSR1_1 | 140 | 144 | PF12202 | 0.255 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 611 | 615 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.389 |
DOC_USP7_UBL2_3 | 87 | 91 | PF12436 | 0.287 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 585 | 590 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 659 | 664 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 295 | 300 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 346 | 355 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 436 | 442 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 465 | 471 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 556 | 562 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 584 | 589 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 607 | 611 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 656 | 661 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 666 | 671 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 687 | 693 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 80 | 84 | PF00244 | 0.315 |
LIG_BRCT_BRCA1_1 | 613 | 617 | PF00533 | 0.622 |
LIG_eIF4E_1 | 118 | 124 | PF01652 | 0.371 |
LIG_EVH1_2 | 310 | 314 | PF00568 | 0.533 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.272 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.574 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.293 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.254 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.401 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.759 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.404 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.404 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.417 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.409 |
LIG_FHA_1 | 687 | 693 | PF00498 | 0.232 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.339 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.255 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.255 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.241 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.557 |
LIG_FHA_2 | 675 | 681 | PF00498 | 0.568 |
LIG_LIR_Apic_2 | 207 | 213 | PF02991 | 0.242 |
LIG_LIR_Apic_2 | 316 | 320 | PF02991 | 0.619 |
LIG_LIR_Apic_2 | 352 | 358 | PF02991 | 0.488 |
LIG_LIR_Apic_2 | 659 | 663 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 116 | 124 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 145 | 156 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 313 | 322 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 614 | 624 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 691 | 702 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.243 |
LIG_LIR_Nem_3 | 313 | 317 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 575 | 581 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 652 | 658 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 691 | 697 | PF02991 | 0.404 |
LIG_MYND_1 | 306 | 310 | PF01753 | 0.457 |
LIG_NRBOX | 131 | 137 | PF00104 | 0.371 |
LIG_NRBOX | 235 | 241 | PF00104 | 0.237 |
LIG_Pex14_2 | 110 | 114 | PF04695 | 0.277 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.253 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.174 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.237 |
LIG_SH2_CRK | 660 | 664 | PF00017 | 0.429 |
LIG_SH2_CRK | 694 | 698 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 660 | 664 | PF00017 | 0.425 |
LIG_SH2_PTP2 | 148 | 151 | PF00017 | 0.315 |
LIG_SH2_PTP2 | 210 | 213 | PF00017 | 0.237 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.404 |
LIG_SH3_2 | 602 | 607 | PF14604 | 0.607 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.237 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.424 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.558 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.651 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.597 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.568 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.531 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.701 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.548 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.417 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.517 |
LIG_SH3_4 | 28 | 35 | PF00018 | 0.501 |
LIG_SH3_CIN85_PxpxPR_1 | 602 | 607 | PF14604 | 0.532 |
LIG_TRAF2_2 | 245 | 250 | PF00917 | 0.237 |
LIG_TYR_ITIM | 235 | 240 | PF00017 | 0.255 |
LIG_TYR_ITIM | 692 | 697 | PF00017 | 0.472 |
LIG_UBA3_1 | 132 | 137 | PF00899 | 0.280 |
LIG_WRC_WIRS_1 | 111 | 116 | PF05994 | 0.255 |
LIG_WRC_WIRS_1 | 314 | 319 | PF05994 | 0.594 |
LIG_WW_3 | 604 | 608 | PF00397 | 0.539 |
MOD_CDC14_SPxK_1 | 588 | 591 | PF00782 | 0.483 |
MOD_CDK_SPK_2 | 388 | 393 | PF00069 | 0.706 |
MOD_CDK_SPK_2 | 418 | 423 | PF00069 | 0.631 |
MOD_CDK_SPxK_1 | 585 | 591 | PF00069 | 0.561 |
MOD_CDK_SPxxK_3 | 281 | 288 | PF00069 | 0.364 |
MOD_CDK_SPxxK_3 | 659 | 666 | PF00069 | 0.429 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.563 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.666 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.414 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.405 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.422 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.315 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.301 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.637 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.291 |
MOD_CK2_1 | 674 | 680 | PF00069 | 0.610 |
MOD_Cter_Amidation | 664 | 667 | PF01082 | 0.299 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.296 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.722 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.574 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.502 |
MOD_GlcNHglycan | 41 | 45 | PF01048 | 0.517 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.716 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.636 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.259 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.295 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.237 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.357 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.360 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.461 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.602 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.710 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.418 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.601 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.502 |
MOD_N-GLC_1 | 516 | 521 | PF02516 | 0.209 |
MOD_N-GLC_1 | 635 | 640 | PF02516 | 0.217 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.286 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.609 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.556 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.394 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.409 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.404 |
MOD_NEK2_1 | 686 | 691 | PF00069 | 0.458 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.485 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.255 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.402 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.461 |
MOD_PK_1 | 139 | 145 | PF00069 | 0.226 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.371 |
MOD_PKA_1 | 200 | 206 | PF00069 | 0.237 |
MOD_PKA_1 | 346 | 352 | PF00069 | 0.601 |
MOD_PKA_1 | 570 | 576 | PF00069 | 0.462 |
MOD_PKA_1 | 666 | 672 | PF00069 | 0.499 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.299 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.237 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.601 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.428 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.615 |
MOD_PKA_2 | 632 | 638 | PF00069 | 0.404 |
MOD_PKA_2 | 666 | 672 | PF00069 | 0.404 |
MOD_PKA_2 | 686 | 692 | PF00069 | 0.231 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.315 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.373 |
MOD_Plk_1 | 635 | 641 | PF00069 | 0.417 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.315 |
MOD_Plk_2-3 | 128 | 134 | PF00069 | 0.371 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.298 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.286 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.254 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.241 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.436 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.352 |
MOD_Plk_4 | 688 | 694 | PF00069 | 0.366 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.287 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.371 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.484 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.668 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.621 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.603 |
MOD_ProDKin_1 | 585 | 591 | PF00069 | 0.517 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.304 |
MOD_ProDKin_1 | 659 | 665 | PF00069 | 0.429 |
MOD_SUMO_for_1 | 537 | 540 | PF00179 | 0.499 |
MOD_SUMO_for_1 | 552 | 555 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 163 | 172 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 193 | 203 | PF00179 | 0.237 |
MOD_SUMO_rev_2 | 214 | 220 | PF00179 | 0.371 |
MOD_SUMO_rev_2 | 567 | 573 | PF00179 | 0.503 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.174 |
TRG_ENDOCYTIC_2 | 694 | 697 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 100 | 102 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.257 |
TRG_ER_diArg_1 | 666 | 668 | PF00400 | 0.492 |
TRG_NES_CRM1_1 | 134 | 145 | PF08389 | 0.371 |
TRG_NES_CRM1_1 | 180 | 193 | PF08389 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 274 | 279 | PF00026 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 622 | 627 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I191 | Leptomonas seymouri | 72% | 95% |
A0A0S4JMY6 | Bodo saltans | 48% | 91% |
A0A1X0NTN5 | Trypanosomatidae | 50% | 93% |
A0A3Q8IAR8 | Leishmania donovani | 97% | 100% |
A0A422N3U8 | Trypanosoma rangeli | 48% | 97% |
A4H913 | Leishmania braziliensis | 91% | 100% |
A4HXE5 | Leishmania infantum | 97% | 100% |
C9ZTW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AR40 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 99% |
P0C8M8 | Zea mays | 38% | 100% |
P32562 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
P50528 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
P53351 | Mus musculus | 30% | 100% |
Q07832 | Mus musculus | 32% | 100% |
Q4FZD7 | Mus musculus | 29% | 100% |
Q62673 | Rattus norvegicus | 32% | 100% |
Q9R012 | Rattus norvegicus | 30% | 100% |