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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4QFK4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.326 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 525 | 527 | PF00675 | 0.597 |
CLV_PCSK_FUR_1 | 456 | 460 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 455 | 457 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 524 | 526 | PF00082 | 0.586 |
CLV_PCSK_PC7_1 | 459 | 465 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.556 |
DOC_CKS1_1 | 384 | 389 | PF01111 | 0.537 |
DOC_CKS1_1 | 393 | 398 | PF01111 | 0.517 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 417 | 426 | PF00134 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 8 | 14 | PF00134 | 0.565 |
DOC_MAPK_gen_1 | 232 | 241 | PF00069 | 0.423 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.238 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.265 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.265 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 440 | 444 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.429 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 403 | 408 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 510 | 515 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 542 | 552 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 599 | 605 | PF00244 | 0.566 |
LIG_APCC_ABBA_1 | 183 | 188 | PF00400 | 0.265 |
LIG_APCC_ABBAyCdc20_2 | 227 | 233 | PF00400 | 0.301 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.482 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.482 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.482 |
LIG_deltaCOP1_diTrp_1 | 338 | 348 | PF00928 | 0.265 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.274 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.202 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.351 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.300 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.606 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.547 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.265 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.262 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.310 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.583 |
LIG_FHA_2 | 619 | 625 | PF00498 | 0.525 |
LIG_LIR_Apic_2 | 204 | 208 | PF02991 | 0.238 |
LIG_LIR_Apic_2 | 271 | 277 | PF02991 | 0.409 |
LIG_LIR_Apic_2 | 427 | 433 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 370 | 379 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 201 | 205 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 370 | 375 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.433 |
LIG_Pex14_1 | 371 | 375 | PF04695 | 0.309 |
LIG_PTAP_UEV_1 | 395 | 400 | PF05743 | 0.493 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.549 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.470 |
LIG_SH2_GRB2like | 173 | 176 | PF00017 | 0.265 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.265 |
LIG_SH2_STAP1 | 593 | 597 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.509 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.506 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.364 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.550 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.527 |
LIG_SUMO_SIM_anti_2 | 158 | 163 | PF11976 | 0.417 |
LIG_SUMO_SIM_anti_2 | 362 | 368 | PF11976 | 0.305 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.265 |
LIG_TRFH_1 | 405 | 409 | PF08558 | 0.525 |
LIG_UBA3_1 | 300 | 307 | PF00899 | 0.193 |
LIG_UBA3_1 | 99 | 103 | PF00899 | 0.327 |
LIG_WRC_WIRS_1 | 202 | 207 | PF05994 | 0.265 |
MOD_CDC14_SPxK_1 | 408 | 411 | PF00782 | 0.512 |
MOD_CDK_SPxK_1 | 405 | 411 | PF00069 | 0.522 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.265 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.193 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.505 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.265 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.588 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.591 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.614 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.661 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.654 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.627 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.581 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.586 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.617 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.543 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.532 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.385 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.270 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.592 |
MOD_CK2_1 | 606 | 612 | PF00069 | 0.567 |
MOD_CK2_1 | 618 | 624 | PF00069 | 0.505 |
MOD_Cter_Amidation | 453 | 456 | PF01082 | 0.592 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.423 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.265 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.554 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.238 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.211 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.281 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.585 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.645 |
MOD_GlcNHglycan | 441 | 445 | PF01048 | 0.572 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.649 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.694 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.666 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.627 |
MOD_GlcNHglycan | 500 | 504 | PF01048 | 0.616 |
MOD_GlcNHglycan | 52 | 56 | PF01048 | 0.551 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.595 |
MOD_GlcNHglycan | 565 | 569 | PF01048 | 0.536 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.569 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.450 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.515 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.405 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.341 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.521 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.663 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.642 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.559 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.599 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.653 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.698 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.631 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.542 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.620 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.569 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.493 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.562 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.552 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.462 |
MOD_LATS_1 | 465 | 471 | PF00433 | 0.542 |
MOD_N-GLC_1 | 420 | 425 | PF02516 | 0.516 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.561 |
MOD_N-GLC_1 | 582 | 587 | PF02516 | 0.523 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.467 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.560 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.269 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.270 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.523 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.297 |
MOD_NEK2_1 | 595 | 600 | PF00069 | 0.517 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.547 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.344 |
MOD_NEK2_2 | 138 | 143 | PF00069 | 0.504 |
MOD_NEK2_2 | 600 | 605 | PF00069 | 0.550 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.265 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.265 |
MOD_PIKK_1 | 478 | 484 | PF00454 | 0.588 |
MOD_PKA_1 | 458 | 464 | PF00069 | 0.579 |
MOD_PKA_1 | 46 | 52 | PF00069 | 0.521 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.387 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.409 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.548 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.522 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.563 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.638 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.622 |
MOD_PKA_2 | 598 | 604 | PF00069 | 0.557 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.386 |
MOD_PKB_1 | 497 | 505 | PF00069 | 0.565 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.373 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.326 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.265 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.234 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.245 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.275 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.583 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.484 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.545 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.697 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.688 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.561 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.549 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.586 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.597 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.554 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.555 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.560 |
MOD_SUMO_for_1 | 142 | 145 | PF00179 | 0.500 |
MOD_SUMO_for_1 | 155 | 158 | PF00179 | 0.184 |
MOD_SUMO_for_1 | 75 | 78 | PF00179 | 0.378 |
MOD_SUMO_rev_2 | 565 | 572 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 622 | 627 | PF00179 | 0.492 |
TRG_DiLeu_BaEn_2 | 343 | 349 | PF01217 | 0.265 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.354 |
TRG_NLS_MonoExtN_4 | 521 | 528 | PF00514 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 172 | 176 | PF00026 | 0.265 |
TRG_Pf-PMV_PEXEL_1 | 232 | 237 | PF00026 | 0.364 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IFW0 | Leishmania donovani | 27% | 100% |
A0A3Q8IRT6 | Leishmania donovani | 25% | 100% |
A0A3Q8IVR8 | Leishmania donovani | 26% | 100% |
A0A3S5H5G0 | Leishmania donovani | 21% | 100% |
A0A3S7WY10 | Leishmania donovani | 22% | 100% |
A0A3S7XAX0 | Leishmania donovani | 25% | 100% |
A4H459 | Leishmania braziliensis | 22% | 100% |
A4H7V0 | Leishmania braziliensis | 77% | 88% |
A4HCD7 | Leishmania braziliensis | 29% | 100% |
A4HHP8 | Leishmania braziliensis | 24% | 100% |
A4HI35 | Leishmania braziliensis | 24% | 100% |
A4HJW2 | Leishmania braziliensis | 27% | 100% |
A4HNT2 | Leishmania braziliensis | 27% | 100% |
A4HNU6 | Leishmania braziliensis | 28% | 100% |
A4HSE2 | Leishmania infantum | 21% | 100% |
A4HW76 | Leishmania infantum | 90% | 78% |
A4I5B1 | Leishmania infantum | 25% | 100% |
A4I7C4 | Leishmania infantum | 27% | 100% |
A4ICR2 | Leishmania infantum | 26% | 100% |
A4IDK3 | Leishmania infantum | 25% | 100% |
E9AH34 | Leishmania infantum | 23% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 21% | 100% |
E9APX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 88% |
E9ASJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ASK6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AT06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AWL2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4Q1J2 | Leishmania major | 25% | 100% |
Q4Q1Z0 | Leishmania major | 26% | 100% |
Q4Q204 | Leishmania major | 26% | 100% |
Q4Q5T9 | Leishmania major | 26% | 100% |
Q4Q7M5 | Leishmania major | 25% | 100% |
Q4QJJ0 | Leishmania major | 21% | 100% |
Q5R4L1 | Pongo abelii | 24% | 92% |
Q9FGW5 | Arabidopsis thaliana | 27% | 100% |
Q9NYY3 | Homo sapiens | 24% | 92% |
Q9R012 | Rattus norvegicus | 24% | 92% |
V5BCN4 | Trypanosoma cruzi | 23% | 100% |