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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HDJ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004672 | protein kinase activity | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 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: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:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0004707 | MAP kinase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.512 |
CLV_C14_Caspase3-7 | 445 | 449 | PF00656 | 0.254 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.294 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.290 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.289 |
CLV_PCSK_PC7_1 | 521 | 527 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.258 |
DEG_SPOP_SBC_1 | 168 | 172 | PF00917 | 0.522 |
DOC_CKS1_1 | 436 | 441 | PF01111 | 0.258 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.676 |
DOC_MAPK_gen_1 | 393 | 402 | PF00069 | 0.322 |
DOC_PP1_RVXF_1 | 413 | 420 | PF00149 | 0.258 |
DOC_PP2B_PxIxI_1 | 535 | 541 | PF00149 | 0.240 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.556 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.664 |
DOC_USP7_MATH_2 | 62 | 68 | PF00917 | 0.605 |
DOC_USP7_UBL2_3 | 34 | 38 | PF12436 | 0.600 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.258 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.287 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 256 | 264 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 327 | 333 | PF00244 | 0.250 |
LIG_14-3-3_CanoR_1 | 35 | 45 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 372 | 379 | PF00244 | 0.296 |
LIG_14-3-3_CanoR_1 | 74 | 81 | PF00244 | 0.618 |
LIG_APCC_ABBA_1 | 344 | 349 | PF00400 | 0.258 |
LIG_BIR_III_4 | 448 | 452 | PF00653 | 0.254 |
LIG_CtBP_PxDLS_1 | 46 | 50 | PF00389 | 0.499 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.628 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.477 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.258 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.396 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.516 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.497 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.262 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.258 |
LIG_Integrin_RGD_1 | 217 | 219 | PF01839 | 0.482 |
LIG_LIR_Apic_2 | 438 | 444 | PF02991 | 0.305 |
LIG_LIR_Apic_2 | 58 | 62 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 238 | 243 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 331 | 335 | PF02991 | 0.264 |
LIG_PTAP_UEV_1 | 482 | 487 | PF05743 | 0.192 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.258 |
LIG_SH2_SRC | 384 | 387 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.258 |
LIG_SH2_STAT3 | 456 | 459 | PF00017 | 0.192 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.305 |
LIG_SH3_1 | 362 | 368 | PF00018 | 0.231 |
LIG_SH3_2 | 477 | 482 | PF14604 | 0.258 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.547 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.622 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.549 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.231 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.690 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.327 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.331 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.595 |
LIG_SUMO_SIM_par_1 | 307 | 313 | PF11976 | 0.250 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.625 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.258 |
LIG_TRAF2_1 | 96 | 99 | PF00917 | 0.452 |
LIG_WRC_WIRS_1 | 329 | 334 | PF05994 | 0.258 |
MOD_CDK_SPK_2 | 67 | 72 | PF00069 | 0.591 |
MOD_CDK_SPxxK_3 | 67 | 74 | PF00069 | 0.632 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.561 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.514 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.258 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.275 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.290 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.595 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.563 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.515 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.463 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.575 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.258 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.565 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.508 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.494 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.676 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.501 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.521 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.450 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.226 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.407 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.623 |
MOD_GlcNHglycan | 448 | 452 | PF01048 | 0.258 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.266 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.264 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.308 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.644 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.630 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.512 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.576 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.401 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.552 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.611 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.296 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.302 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.312 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.350 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.319 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.523 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.305 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.583 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.563 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.373 |
MOD_N-GLC_2 | 328 | 330 | PF02516 | 0.258 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.487 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.390 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.297 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.286 |
MOD_NEK2_2 | 284 | 289 | PF00069 | 0.258 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.333 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.207 |
MOD_PIKK_1 | 409 | 415 | PF00454 | 0.255 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.226 |
MOD_PK_1 | 107 | 113 | PF00069 | 0.472 |
MOD_PKA_1 | 106 | 112 | PF00069 | 0.470 |
MOD_PKA_1 | 36 | 42 | PF00069 | 0.611 |
MOD_PKA_1 | 423 | 429 | PF00069 | 0.258 |
MOD_PKA_1 | 525 | 531 | PF00069 | 0.258 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.719 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.502 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.299 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.646 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.258 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.239 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.305 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.626 |
MOD_PKB_1 | 105 | 113 | PF00069 | 0.470 |
MOD_PKB_1 | 35 | 43 | PF00069 | 0.518 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.609 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.616 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.472 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.249 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.274 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.322 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.512 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.305 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.483 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.522 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.543 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.481 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.258 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.287 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.704 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.593 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.258 |
TRG_ER_diArg_1 | 105 | 107 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.258 |
TRG_NES_CRM1_1 | 304 | 317 | PF08389 | 0.258 |
TRG_NLS_MonoCore_2 | 33 | 38 | PF00514 | 0.506 |
TRG_NLS_MonoExtC_3 | 33 | 38 | PF00514 | 0.506 |
TRG_NLS_MonoExtC_3 | 360 | 365 | PF00514 | 0.258 |
TRG_NLS_MonoExtN_4 | 34 | 40 | PF00514 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.258 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTF0 | Leptomonas seymouri | 62% | 86% |
A0A3Q8ICW9 | Leishmania donovani | 80% | 90% |
A0A3Q8IH39 | Leishmania donovani | 22% | 100% |
A0A3Q8IIG1 | Leishmania donovani | 28% | 100% |
A0A3Q8ITZ9 | Leishmania donovani | 26% | 100% |
A0A3Q8IVR8 | Leishmania donovani | 26% | 100% |
A0A3R7JV29 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H5G0 | Leishmania donovani | 25% | 100% |
A0A3S5H789 | Leishmania donovani | 24% | 100% |
A0A3S7WRG1 | Leishmania donovani | 24% | 100% |
A0A3S7WTN9 | Leishmania donovani | 25% | 100% |
A0A3S7X2W3 | Leishmania donovani | 29% | 100% |
A0A3S7X7Y2 | Leishmania donovani | 29% | 100% |
A0A3S7XA45 | Leishmania donovani | 27% | 100% |
A4H3J3 | Leishmania braziliensis | 26% | 100% |
A4H459 | Leishmania braziliensis | 26% | 100% |
A4H601 | Leishmania braziliensis | 23% | 100% |
A4H8C4 | Leishmania braziliensis | 25% | 100% |
A4HA94 | Leishmania braziliensis | 26% | 100% |
A4HAS1 | Leishmania braziliensis | 28% | 100% |
A4HFA1 | Leishmania braziliensis | 26% | 100% |
A4HH03 | Leishmania braziliensis | 29% | 100% |
A4HHN1 | Leishmania braziliensis | 28% | 100% |
A4HLJ9 | Leishmania braziliensis | 25% | 100% |
A4HNG3 | Leishmania braziliensis | 26% | 100% |
A4HNT2 | Leishmania braziliensis | 25% | 100% |
A4HSE2 | Leishmania infantum | 25% | 100% |
A4HUC8 | Leishmania infantum | 22% | 100% |
A4HUS3 | Leishmania infantum | 24% | 100% |
A4HWP5 | Leishmania infantum | 25% | 100% |
A4HYH4 | Leishmania infantum | 28% | 100% |
A4HYX6 | Leishmania infantum | 24% | 100% |
A4I0Y4 | Leishmania infantum | 80% | 90% |
A4I435 | Leishmania infantum | 28% | 100% |
A4I4U6 | Leishmania infantum | 30% | 100% |
A4I910 | Leishmania infantum | 26% | 100% |
A4I9Y5 | Leishmania infantum | 29% | 100% |
A4IC54 | Leishmania infantum | 27% | 100% |
A4ICR2 | Leishmania infantum | 26% | 100% |
A7A1P0 | Saccharomyces cerevisiae (strain YJM789) | 29% | 76% |
B5VNQ3 | Saccharomyces cerevisiae (strain AWRI1631) | 30% | 76% |
E9AFX4 | Leishmania major | 27% | 100% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ALJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AN28 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9ANF7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9AS98 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9ASJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9AWZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 90% |
E9B0C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B3X5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B4Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B727 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
P23561 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 76% |
P36507 | Homo sapiens | 26% | 100% |
Q4Q204 | Leishmania major | 26% | 100% |
Q4Q2Z2 | Leishmania major | 29% | 100% |
Q4Q449 | Leishmania major | 26% | 100% |
Q4Q7W2 | Leishmania major | 27% | 100% |
Q4QAI6 | Leishmania major | 79% | 100% |
Q4QD66 | Leishmania major | 28% | 100% |
Q4QF23 | Leishmania major | 24% | 100% |
Q4QH69 | Leishmania major | 24% | 100% |
Q4QHJ8 | Leishmania major | 22% | 100% |
Q4QJJ0 | Leishmania major | 25% | 100% |
Q6BVA0 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 27% | 100% |
Q6F3A6 | Oryza sativa subsp. japonica | 26% | 91% |
Q9U6V4 | Leishmania donovani | 28% | 100% |
Q9Y077 | Leishmania major | 30% | 100% |