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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: E9B2Y6
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0055085 | transmembrane transport | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0005215 | transporter activity | 1 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0022804 | active transmembrane transporter activity | 3 | 9 |
GO:0022857 | transmembrane transporter activity | 2 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140359 | ABC-type transporter activity | 3 | 9 |
GO:0140657 | ATP-dependent activity | 1 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.280 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.625 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.416 |
DEG_APCC_DBOX_1 | 415 | 423 | PF00400 | 0.644 |
DEG_APCC_DBOX_1 | 655 | 663 | PF00400 | 0.537 |
DEG_SCF_FBW7_2 | 214 | 221 | PF00400 | 0.591 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.509 |
DOC_CKS1_1 | 215 | 220 | PF01111 | 0.604 |
DOC_CYCLIN_RxL_1 | 170 | 178 | PF00134 | 0.167 |
DOC_MAPK_FxFP_2 | 470 | 473 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 134 | 144 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 553 | 561 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 134 | 142 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 173 | 181 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 683 | 690 | PF00069 | 0.609 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.518 |
DOC_PP4_FxxP_1 | 470 | 473 | PF00568 | 0.586 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.425 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 214 | 219 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.359 |
LIG_14-3-3_CanoR_1 | 240 | 249 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 320 | 325 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 36 | 42 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 416 | 420 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 421 | 426 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 430 | 435 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 618 | 625 | PF00244 | 0.499 |
LIG_Actin_WH2_2 | 401 | 418 | PF00022 | 0.469 |
LIG_Actin_WH2_2 | 682 | 699 | PF00022 | 0.606 |
LIG_APCC_ABBA_1 | 163 | 168 | PF00400 | 0.408 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.761 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.416 |
LIG_BRCT_BRCA1_1 | 633 | 637 | PF00533 | 0.525 |
LIG_Clathr_ClatBox_1 | 671 | 675 | PF01394 | 0.502 |
LIG_EH_1 | 634 | 638 | PF12763 | 0.525 |
LIG_eIF4E_1 | 184 | 190 | PF01652 | 0.416 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.458 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.394 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.556 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.372 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.553 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.587 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.228 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.577 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.502 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.539 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.367 |
LIG_FHA_1 | 676 | 682 | PF00498 | 0.560 |
LIG_FHA_1 | 701 | 707 | PF00498 | 0.534 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.460 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.556 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.618 |
LIG_FHA_2 | 437 | 443 | PF00498 | 0.705 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.460 |
LIG_FHA_2 | 610 | 616 | PF00498 | 0.520 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.502 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.594 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.577 |
LIG_LIR_Apic_2 | 469 | 473 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 612 | 620 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 634 | 644 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 666 | 677 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 612 | 616 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 634 | 640 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 666 | 672 | PF02991 | 0.521 |
LIG_LYPXL_yS_3 | 472 | 475 | PF13949 | 0.578 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.416 |
LIG_SH2_CRK | 669 | 673 | PF00017 | 0.521 |
LIG_SH2_NCK_1 | 358 | 362 | PF00017 | 0.416 |
LIG_SH2_SRC | 166 | 169 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 669 | 673 | PF00017 | 0.521 |
LIG_SH2_STAT3 | 379 | 382 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.335 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.423 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.701 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.570 |
LIG_SH3_3 | 593 | 599 | PF00018 | 0.575 |
LIG_SH3_3 | 601 | 607 | PF00018 | 0.481 |
LIG_SH3_3 | 641 | 647 | PF00018 | 0.575 |
LIG_SUMO_SIM_anti_2 | 178 | 183 | PF11976 | 0.178 |
LIG_SUMO_SIM_anti_2 | 221 | 227 | PF11976 | 0.604 |
LIG_SUMO_SIM_anti_2 | 275 | 280 | PF11976 | 0.416 |
LIG_SUMO_SIM_anti_2 | 366 | 372 | PF11976 | 0.416 |
LIG_SUMO_SIM_anti_2 | 670 | 676 | PF11976 | 0.502 |
LIG_SUMO_SIM_anti_2 | 684 | 691 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 433 | 439 | PF11976 | 0.638 |
LIG_SUMO_SIM_par_1 | 451 | 458 | PF11976 | 0.625 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 670 | 676 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 702 | 708 | PF11976 | 0.548 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.622 |
LIG_UBA3_1 | 689 | 694 | PF00899 | 0.547 |
LIG_WRC_WIRS_1 | 143 | 148 | PF05994 | 0.270 |
LIG_WRC_WIRS_1 | 398 | 403 | PF05994 | 0.372 |
LIG_WRC_WIRS_1 | 581 | 586 | PF05994 | 0.520 |
LIG_WRC_WIRS_1 | 637 | 642 | PF05994 | 0.575 |
MOD_CDK_SPxxK_3 | 8 | 15 | PF00069 | 0.658 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.762 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.593 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.617 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.334 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.569 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.373 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.364 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.537 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.507 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.566 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.577 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.622 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.709 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.474 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.419 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.520 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.537 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.631 |
MOD_CK2_1 | 723 | 729 | PF00069 | 0.714 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.510 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.646 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.524 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.389 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.591 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.365 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.404 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.392 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.379 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.323 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.278 |
MOD_GlcNHglycan | 590 | 594 | PF01048 | 0.299 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.208 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.337 |
MOD_GlcNHglycan | 649 | 652 | PF01048 | 0.260 |
MOD_GlcNHglycan | 682 | 686 | PF01048 | 0.389 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.481 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.547 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.657 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.742 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.525 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.139 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.501 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.425 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.401 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.733 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.513 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.529 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.548 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.746 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.416 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.521 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.533 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.571 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.399 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.499 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.378 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.292 |
MOD_N-GLC_1 | 721 | 726 | PF02516 | 0.267 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.335 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.259 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.554 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.358 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.368 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.615 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.541 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.597 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.597 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.435 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.308 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.400 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.570 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.721 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.290 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.502 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.502 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.424 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.568 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.528 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.668 |
MOD_OFUCOSY | 532 | 537 | PF10250 | 0.375 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.469 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.651 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.733 |
MOD_PIKK_1 | 509 | 515 | PF00454 | 0.474 |
MOD_PIKK_1 | 551 | 557 | PF00454 | 0.537 |
MOD_PKA_1 | 618 | 624 | PF00069 | 0.537 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.598 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.593 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.340 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.609 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.537 |
MOD_PKA_2 | 696 | 702 | PF00069 | 0.647 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.567 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.436 |
MOD_Plk_1 | 589 | 595 | PF00069 | 0.388 |
MOD_Plk_1 | 667 | 673 | PF00069 | 0.527 |
MOD_Plk_1 | 681 | 687 | PF00069 | 0.612 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.389 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.369 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.578 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.588 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.364 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.371 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.357 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.505 |
MOD_Plk_4 | 667 | 673 | PF00069 | 0.501 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.556 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.719 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.413 |
MOD_ProDKin_1 | 214 | 220 | PF00069 | 0.600 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.422 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.760 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.362 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.416 |
TRG_DiLeu_BaLyEn_6 | 536 | 541 | PF01217 | 0.537 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.620 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 669 | 672 | PF00928 | 0.521 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 240 | 244 | PF00026 | 0.421 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7P4 | Leptomonas seymouri | 62% | 100% |
A0A0S4J6G3 | Bodo saltans | 29% | 100% |
A0A1X0NU80 | Trypanosomatidae | 35% | 100% |
A0A3S5H7S2 | Leishmania donovani | 89% | 99% |
A4HKJ6 | Leishmania braziliensis | 78% | 99% |
A4I828 | Leishmania infantum | 88% | 99% |
E9AD24 | Leishmania major | 23% | 100% |
Q2NUA5 | Sodalis glossinidius (strain morsitans) | 23% | 100% |
Q4Q570 | Leishmania major | 89% | 100% |
Q9NRK6 | Homo sapiens | 25% | 99% |