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:0030117 | membrane coat | 3 | 10 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0030119 | AP-type membrane coat adaptor complex | 3 | 2 |
GO:0030131 | clathrin adaptor complex | 4 | 2 |
Related structures:
AlphaFold database: A4HQJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 8 |
GO:0005515 | protein binding | 2 | 8 |
GO:0030276 | clathrin binding | 3 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 569 | 573 | PF00656 | 0.426 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.170 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.165 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.277 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 553 | 555 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.243 |
CLV_PCSK_PC1ET2_1 | 54 | 56 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 721 | 725 | PF00082 | 0.500 |
CLV_Separin_Fungi | 716 | 722 | PF03568 | 0.492 |
CLV_Separin_Metazoa | 143 | 147 | PF03568 | 0.258 |
CLV_Separin_Metazoa | 387 | 391 | PF03568 | 0.326 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.170 |
DEG_APCC_DBOX_1 | 492 | 500 | PF00400 | 0.389 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.444 |
DOC_CDC14_PxL_1 | 690 | 698 | PF14671 | 0.515 |
DOC_CKS1_1 | 360 | 365 | PF01111 | 0.259 |
DOC_CKS1_1 | 622 | 627 | PF01111 | 0.684 |
DOC_CYCLIN_RxL_1 | 350 | 362 | PF00134 | 0.258 |
DOC_CYCLIN_RxL_1 | 97 | 109 | PF00134 | 0.305 |
DOC_MAPK_DCC_7 | 342 | 351 | PF00069 | 0.243 |
DOC_MAPK_gen_1 | 157 | 164 | PF00069 | 0.268 |
DOC_MAPK_gen_1 | 181 | 187 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 350 | 360 | PF00069 | 0.243 |
DOC_MAPK_gen_1 | 433 | 441 | PF00069 | 0.243 |
DOC_MAPK_gen_1 | 85 | 92 | PF00069 | 0.243 |
DOC_MAPK_HePTP_8 | 316 | 328 | PF00069 | 0.243 |
DOC_MAPK_HePTP_8 | 339 | 351 | PF00069 | 0.170 |
DOC_MAPK_MEF2A_6 | 127 | 134 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.243 |
DOC_MAPK_MEF2A_6 | 342 | 351 | PF00069 | 0.243 |
DOC_MAPK_MEF2A_6 | 353 | 360 | PF00069 | 0.243 |
DOC_MAPK_MEF2A_6 | 390 | 399 | PF00069 | 0.247 |
DOC_MAPK_MEF2A_6 | 433 | 440 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 64 | 73 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 85 | 92 | PF00069 | 0.277 |
DOC_MAPK_NFAT4_5 | 353 | 361 | PF00069 | 0.243 |
DOC_MAPK_RevD_3 | 71 | 86 | PF00069 | 0.243 |
DOC_PP2B_LxvP_1 | 679 | 682 | PF13499 | 0.467 |
DOC_PP2B_LxvP_1 | 696 | 699 | PF13499 | 0.473 |
DOC_PP4_FxxP_1 | 590 | 593 | PF00568 | 0.370 |
DOC_PP4_FxxP_1 | 597 | 600 | PF00568 | 0.389 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.243 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.659 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.550 |
DOC_USP7_UBL2_3 | 50 | 54 | PF12436 | 0.246 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.243 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.170 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.259 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 630 | 635 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 684 | 689 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 133 | 138 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 157 | 164 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 264 | 272 | PF00244 | 0.246 |
LIG_14-3-3_CanoR_1 | 294 | 298 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.256 |
LIG_14-3-3_CanoR_1 | 568 | 576 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 592 | 598 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 721 | 726 | PF00244 | 0.764 |
LIG_Actin_WH2_2 | 130 | 148 | PF00022 | 0.258 |
LIG_Actin_WH2_2 | 344 | 361 | PF00022 | 0.305 |
LIG_Actin_WH2_2 | 567 | 582 | PF00022 | 0.431 |
LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_1 | 66 | 70 | PF00533 | 0.258 |
LIG_BRCT_BRCA1_1 | 686 | 690 | PF00533 | 0.632 |
LIG_Clathr_ClatBox_1 | 438 | 442 | PF01394 | 0.337 |
LIG_EVH1_1 | 621 | 625 | PF00568 | 0.509 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.337 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.363 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.169 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.387 |
LIG_FHA_1 | 704 | 710 | PF00498 | 0.798 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.389 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.380 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.368 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.489 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.686 |
LIG_FHA_2 | 706 | 712 | PF00498 | 0.655 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.337 |
LIG_GBD_Chelix_1 | 134 | 142 | PF00786 | 0.170 |
LIG_LIR_Apic_2 | 596 | 600 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 345 | 356 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 468 | 473 | PF02991 | 0.243 |
LIG_LIR_Gen_1 | 591 | 601 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 65 | 76 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 674 | 684 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 468 | 472 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 591 | 597 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 674 | 679 | PF02991 | 0.672 |
LIG_LYPXL_yS_3 | 435 | 438 | PF13949 | 0.246 |
LIG_MAD2 | 555 | 563 | PF02301 | 0.514 |
LIG_MLH1_MIPbox_1 | 22 | 26 | PF16413 | 0.444 |
LIG_MYND_1 | 418 | 422 | PF01753 | 0.258 |
LIG_NRBOX | 183 | 189 | PF00104 | 0.258 |
LIG_NRBOX | 353 | 359 | PF00104 | 0.258 |
LIG_NRBOX | 516 | 522 | PF00104 | 0.312 |
LIG_PCNA_yPIPBox_3 | 294 | 307 | PF02747 | 0.296 |
LIG_Pex14_1 | 234 | 238 | PF04695 | 0.302 |
LIG_SH2_NCK_1 | 343 | 347 | PF00017 | 0.305 |
LIG_SH2_SRC | 89 | 92 | PF00017 | 0.243 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.243 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.304 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.243 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.612 |
LIG_SH3_3 | 675 | 681 | PF00018 | 0.462 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.740 |
LIG_SUMO_SIM_anti_2 | 183 | 190 | PF11976 | 0.341 |
LIG_SUMO_SIM_anti_2 | 334 | 340 | PF11976 | 0.170 |
LIG_SUMO_SIM_par_1 | 103 | 109 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 437 | 443 | PF11976 | 0.294 |
LIG_TRAF2_1 | 454 | 457 | PF00917 | 0.170 |
LIG_TRFH_1 | 140 | 144 | PF08558 | 0.258 |
LIG_TYR_ITIM | 66 | 71 | PF00017 | 0.389 |
LIG_TYR_ITIM | 87 | 92 | PF00017 | 0.243 |
LIG_UBA3_1 | 174 | 182 | PF00899 | 0.337 |
LIG_UBA3_1 | 394 | 398 | PF00899 | 0.277 |
LIG_UBA3_1 | 409 | 417 | PF00899 | 0.139 |
LIG_UBA3_1 | 520 | 526 | PF00899 | 0.170 |
LIG_WRC_WIRS_1 | 107 | 112 | PF05994 | 0.243 |
LIG_WRC_WIRS_1 | 594 | 599 | PF05994 | 0.368 |
MOD_CDK_SPxxK_3 | 115 | 122 | PF00069 | 0.243 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.333 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.348 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.277 |
MOD_CK1_1 | 582 | 588 | PF00069 | 0.415 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.663 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.316 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.389 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.341 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.337 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.337 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.337 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.395 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.243 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.690 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.641 |
MOD_GlcNHglycan | 729 | 732 | PF01048 | 0.706 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.258 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.467 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.255 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.389 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.466 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.577 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.729 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.266 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.337 |
MOD_N-GLC_1 | 58 | 63 | PF02516 | 0.337 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.258 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.473 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.189 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.420 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.326 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.170 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.170 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.395 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.170 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.361 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.277 |
MOD_PIKK_1 | 626 | 632 | PF00454 | 0.749 |
MOD_PIKK_1 | 736 | 742 | PF00454 | 0.618 |
MOD_PK_1 | 133 | 139 | PF00069 | 0.302 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.258 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.216 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.350 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.256 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.618 |
MOD_PKB_1 | 719 | 727 | PF00069 | 0.499 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.243 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.450 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.275 |
MOD_Plk_2-3 | 572 | 578 | PF00069 | 0.415 |
MOD_Plk_2-3 | 610 | 616 | PF00069 | 0.590 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.243 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.389 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.311 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.277 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.200 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.316 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.374 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.325 |
MOD_Plk_4 | 593 | 599 | PF00069 | 0.402 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.302 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.243 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.170 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.259 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.614 |
MOD_ProDKin_1 | 630 | 636 | PF00069 | 0.565 |
MOD_ProDKin_1 | 684 | 690 | PF00069 | 0.656 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.652 |
MOD_SUMO_for_1 | 349 | 352 | PF00179 | 0.243 |
MOD_SUMO_rev_2 | 451 | 461 | PF00179 | 0.284 |
MOD_SUMO_rev_2 | 572 | 582 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 79 | 87 | PF00179 | 0.389 |
TRG_AP2beta_CARGO_1 | 345 | 355 | PF09066 | 0.305 |
TRG_DiLeu_BaEn_1 | 352 | 357 | PF01217 | 0.243 |
TRG_DiLeu_BaEn_1 | 83 | 88 | PF01217 | 0.243 |
TRG_DiLeu_BaEn_2 | 467 | 473 | PF01217 | 0.243 |
TRG_DiLeu_BaLyEn_6 | 539 | 544 | PF01217 | 0.243 |
TRG_DiLeu_LyEn_5 | 352 | 357 | PF01217 | 0.258 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.767 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.243 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 307 | 309 | PF00400 | 0.170 |
TRG_NES_CRM1_1 | 495 | 509 | PF08389 | 0.352 |
TRG_NLS_Bipartite_1 | 30 | 52 | PF00514 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 707 | 711 | PF00026 | 0.512 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7B0 | Leptomonas seymouri | 80% | 100% |
A0A0N1IC81 | Leptomonas seymouri | 26% | 96% |
A0A0S4IS43 | Bodo saltans | 32% | 79% |
A0A0S4J8G3 | Bodo saltans | 26% | 100% |
A0A0S4JSJ9 | Bodo saltans | 58% | 76% |
A0A1X0NL72 | Trypanosomatidae | 64% | 77% |
A0A1X0NUY1 | Trypanosomatidae | 31% | 81% |
A0A1X0P0E5 | Trypanosomatidae | 26% | 95% |
A0A3Q8I939 | Leishmania donovani | 28% | 75% |
A0A3Q8IK57 | Leishmania donovani | 87% | 100% |
A0A3R7L5L0 | Trypanosoma rangeli | 29% | 82% |
A0A3S5IS14 | Trypanosoma rangeli | 58% | 78% |
A0A422NKG4 | Trypanosoma rangeli | 27% | 96% |
A4HV08 | Leishmania infantum | 28% | 75% |
A4ICB7 | Leishmania infantum | 86% | 100% |
D0A3P8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
D0A442 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 97% |
E9AUB2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
O00203 | Homo sapiens | 25% | 68% |
O13939 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
O35643 | Mus musculus | 37% | 79% |
O43005 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
O43079 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
O81742 | Arabidopsis thaliana | 37% | 84% |
P27351 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
P36000 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
P46682 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 92% |
P52303 | Rattus norvegicus | 37% | 79% |
P62944 | Rattus norvegicus | 36% | 80% |
P63009 | Bos taurus | 36% | 80% |
P63010 | Homo sapiens | 36% | 80% |
Q08DS7 | Bos taurus | 36% | 78% |
Q10567 | Homo sapiens | 38% | 79% |
Q13367 | Homo sapiens | 26% | 69% |
Q22498 | Caenorhabditis elegans | 20% | 86% |
Q32PG1 | Bos taurus | 25% | 69% |
Q4Q078 | Leishmania major | 85% | 100% |
Q54R84 | Dictyostelium discoideum | 26% | 89% |
Q54X82 | Dictyostelium discoideum | 38% | 79% |
Q759E2 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 23% | 96% |
Q7YRF1 | Canis lupus familiaris | 25% | 68% |
Q9DBG3 | Mus musculus | 36% | 80% |
Q9JME5 | Mus musculus | 26% | 69% |
Q9LDK9 | Arabidopsis thaliana | 27% | 89% |
Q9SUS3 | Arabidopsis thaliana | 37% | 83% |
Q9WV76 | Mus musculus | 28% | 100% |
Q9Y6B7 | Homo sapiens | 27% | 100% |
Q9Z1T1 | Mus musculus | 25% | 68% |
V5BRU9 | Trypanosoma cruzi | 31% | 82% |
V5BTB0 | Trypanosoma cruzi | 25% | 96% |
V5DDV1 | Trypanosoma cruzi | 58% | 78% |