Highly similar to mitochondrial ADP/ATP antiporters of other Eukaryotes.. Only duplicated sporadically in Strigomonas and T. cruzi.. Localization: Mitochondrial inner membrane (by homology)
| 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: 13 |
| NetGPI | no | yes: 0, no: 13 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005743 | mitochondrial inner membrane | 5 | 14 |
| GO:0016020 | membrane | 2 | 14 |
| GO:0019866 | organelle inner membrane | 4 | 14 |
| GO:0031090 | organelle membrane | 3 | 14 |
| GO:0031966 | mitochondrial membrane | 4 | 14 |
| GO:0110165 | cellular anatomical entity | 1 | 14 |
Related structures:
AlphaFold database: Q4QIN9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006810 | transport | 3 | 14 |
| GO:0006811 | monoatomic ion transport | 4 | 14 |
| GO:0006820 | monoatomic anion transport | 5 | 14 |
| GO:0006862 | nucleotide transport | 6 | 14 |
| GO:0006996 | organelle organization | 4 | 2 |
| GO:0007005 | mitochondrion organization | 5 | 2 |
| GO:0007006 | mitochondrial membrane organization | 5 | 2 |
| GO:0009966 | regulation of signal transduction | 4 | 2 |
| GO:0009968 | negative regulation of signal transduction | 5 | 2 |
| GO:0009987 | cellular process | 1 | 14 |
| GO:0010639 | negative regulation of organelle organization | 6 | 2 |
| GO:0010646 | regulation of cell communication | 4 | 2 |
| GO:0010648 | negative regulation of cell communication | 5 | 2 |
| GO:0010821 | regulation of mitochondrion organization | 6 | 2 |
| GO:0010823 | negative regulation of mitochondrion organization | 7 | 2 |
| GO:0010941 | regulation of cell death | 4 | 2 |
| GO:0015711 | organic anion transport | 5 | 14 |
| GO:0015748 | organophosphate ester transport | 5 | 14 |
| GO:0015865 | purine nucleotide transport | 7 | 14 |
| GO:0015866 | ADP transport | 6 | 14 |
| GO:0015867 | ATP transport | 6 | 14 |
| GO:0015868 | purine ribonucleotide transport | 6 | 14 |
| GO:0015931 | nucleobase-containing compound transport | 5 | 14 |
| GO:0016043 | cellular component organization | 3 | 2 |
| GO:0023051 | regulation of signaling | 3 | 2 |
| GO:0023057 | negative regulation of signaling | 4 | 2 |
| GO:0032879 | regulation of localization | 3 | 2 |
| GO:0033043 | regulation of organelle organization | 5 | 2 |
| GO:0034220 | monoatomic ion transmembrane transport | 3 | 14 |
| GO:0035795 | negative regulation of mitochondrial membrane permeability | 5 | 2 |
| GO:0042981 | regulation of apoptotic process | 6 | 2 |
| GO:0043066 | negative regulation of apoptotic process | 7 | 2 |
| GO:0043067 | regulation of programmed cell death | 5 | 2 |
| GO:0043069 | negative regulation of programmed cell death | 6 | 2 |
| GO:0046902 | regulation of mitochondrial membrane permeability | 4 | 2 |
| GO:0048519 | negative regulation of biological process | 3 | 2 |
| GO:0048523 | negative regulation of cellular process | 4 | 2 |
| GO:0048583 | regulation of response to stimulus | 3 | 2 |
| GO:0048585 | negative regulation of response to stimulus | 4 | 2 |
| GO:0050789 | regulation of biological process | 2 | 2 |
| GO:0050794 | regulation of cellular process | 3 | 2 |
| GO:0051049 | regulation of transport | 4 | 2 |
| GO:0051128 | regulation of cellular component organization | 4 | 2 |
| GO:0051129 | negative regulation of cellular component organization | 5 | 2 |
| GO:0051179 | localization | 1 | 14 |
| GO:0051234 | establishment of localization | 2 | 14 |
| GO:0051503 | adenine nucleotide transport | 8 | 14 |
| GO:0055085 | transmembrane transport | 2 | 14 |
| GO:0060548 | negative regulation of cell death | 5 | 2 |
| GO:0061024 | membrane organization | 4 | 2 |
| GO:0065007 | biological regulation | 1 | 2 |
| GO:0065008 | regulation of biological quality | 2 | 2 |
| GO:0071702 | organic substance transport | 4 | 14 |
| GO:0071705 | nitrogen compound transport | 4 | 14 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
| GO:0072530 | purine-containing compound transmembrane transport | 3 | 14 |
| GO:0090559 | regulation of membrane permeability | 3 | 2 |
| GO:0098656 | monoatomic anion transmembrane transport | 4 | 14 |
| GO:0140021 | mitochondrial ADP transmembrane transport | 4 | 14 |
| GO:1901028 | regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway | 5 | 2 |
| GO:1901029 | negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway | 6 | 2 |
| GO:1901264 | carbohydrate derivative transport | 5 | 14 |
| GO:1901679 | nucleotide transmembrane transport | 3 | 14 |
| GO:1905709 | negative regulation of membrane permeability | 4 | 2 |
| GO:1990542 | mitochondrial transmembrane transport | 3 | 14 |
| GO:1990544 | mitochondrial ATP transmembrane transport | 4 | 14 |
| GO:2001233 | regulation of apoptotic signaling pathway | 5 | 2 |
| GO:2001234 | negative regulation of apoptotic signaling pathway | 6 | 2 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000295 | adenine nucleotide transmembrane transporter activity | 6 | 14 |
| GO:0005215 | transporter activity | 1 | 14 |
| GO:0005346 | purine ribonucleotide transmembrane transporter activity | 4 | 14 |
| GO:0005347 | ATP transmembrane transporter activity | 5 | 14 |
| GO:0005471 | ATP:ADP antiporter activity | 5 | 14 |
| GO:0008509 | monoatomic anion transmembrane transporter activity | 4 | 14 |
| GO:0008514 | organic anion transmembrane transporter activity | 5 | 14 |
| GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 14 |
| GO:0015215 | nucleotide transmembrane transporter activity | 4 | 14 |
| GO:0015216 | purine nucleotide transmembrane transporter activity | 5 | 14 |
| GO:0015217 | ADP transmembrane transporter activity | 5 | 14 |
| GO:0015291 | secondary active transmembrane transporter activity | 4 | 14 |
| GO:0015297 | antiporter activity | 5 | 14 |
| GO:0015605 | organophosphate ester transmembrane transporter activity | 3 | 14 |
| GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 14 |
| GO:0022804 | active transmembrane transporter activity | 3 | 14 |
| GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 14 |
| GO:0022857 | transmembrane transporter activity | 2 | 14 |
| GO:0140323 | obsolete solute:monoatomic anion antiporter activity | 6 | 14 |
| GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 14 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_MEL_PAP_1 | 212 | 218 | PF00089 | 0.203 |
| CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.467 |
| CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.403 |
| CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.284 |
| CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.400 |
| CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.278 |
| CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.319 |
| DEG_APCC_DBOX_1 | 139 | 147 | PF00400 | 0.403 |
| DEG_APCC_DBOX_1 | 89 | 97 | PF00400 | 0.519 |
| DEG_MDM2_SWIB_1 | 119 | 126 | PF02201 | 0.519 |
| DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.712 |
| DOC_MAPK_gen_1 | 205 | 212 | PF00069 | 0.437 |
| DOC_MAPK_gen_1 | 307 | 314 | PF00069 | 0.484 |
| DOC_MAPK_MEF2A_6 | 205 | 212 | PF00069 | 0.420 |
| DOC_MAPK_MEF2A_6 | 307 | 314 | PF00069 | 0.484 |
| DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.326 |
| DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.679 |
| DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.450 |
| DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.640 |
| DOC_USP7_MATH_2 | 272 | 278 | PF00917 | 0.390 |
| DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.279 |
| LIG_14-3-3_CanoR_1 | 223 | 227 | PF00244 | 0.445 |
| LIG_14-3-3_CanoR_1 | 243 | 248 | PF00244 | 0.117 |
| LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.757 |
| LIG_14-3-3_CanoR_1 | 318 | 328 | PF00244 | 0.433 |
| LIG_BRCT_BRCA1_1 | 164 | 168 | PF00533 | 0.329 |
| LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.427 |
| LIG_Clathr_ClatBox_1 | 73 | 77 | PF01394 | 0.624 |
| LIG_CtBP_PxDLS_1 | 302 | 306 | PF00389 | 0.519 |
| LIG_eIF4E_1 | 242 | 248 | PF01652 | 0.319 |
| LIG_FHA_1 | 1 | 7 | PF00498 | 0.680 |
| LIG_FHA_1 | 244 | 250 | PF00498 | 0.352 |
| LIG_FHA_1 | 278 | 284 | PF00498 | 0.250 |
| LIG_FHA_1 | 293 | 299 | PF00498 | 0.198 |
| LIG_FHA_1 | 343 | 349 | PF00498 | 0.350 |
| LIG_FHA_1 | 353 | 359 | PF00498 | 0.283 |
| LIG_LIR_Gen_1 | 121 | 129 | PF02991 | 0.464 |
| LIG_LIR_Gen_1 | 183 | 192 | PF02991 | 0.321 |
| LIG_LIR_Gen_1 | 202 | 210 | PF02991 | 0.429 |
| LIG_LIR_Gen_1 | 252 | 263 | PF02991 | 0.286 |
| LIG_LIR_Gen_1 | 47 | 56 | PF02991 | 0.597 |
| LIG_LIR_Nem_3 | 118 | 122 | PF02991 | 0.499 |
| LIG_LIR_Nem_3 | 183 | 187 | PF02991 | 0.321 |
| LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.447 |
| LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.474 |
| LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.306 |
| LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.601 |
| LIG_Pex14_2 | 119 | 123 | PF04695 | 0.446 |
| LIG_Pex14_2 | 222 | 226 | PF04695 | 0.519 |
| LIG_REV1ctd_RIR_1 | 338 | 346 | PF16727 | 0.487 |
| LIG_SH2_CRK | 184 | 188 | PF00017 | 0.323 |
| LIG_SH2_CRK | 242 | 246 | PF00017 | 0.287 |
| LIG_SH2_CRK | 255 | 259 | PF00017 | 0.216 |
| LIG_SH2_CRK | 48 | 52 | PF00017 | 0.677 |
| LIG_SH2_NCK_1 | 179 | 183 | PF00017 | 0.318 |
| LIG_SH2_PTP2 | 269 | 272 | PF00017 | 0.406 |
| LIG_SH2_SRC | 229 | 232 | PF00017 | 0.403 |
| LIG_SH2_SRC | 269 | 272 | PF00017 | 0.413 |
| LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.293 |
| LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.463 |
| LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.487 |
| LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.367 |
| LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.505 |
| LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.519 |
| LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.289 |
| LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.351 |
| LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.547 |
| LIG_SH3_3 | 156 | 162 | PF00018 | 0.264 |
| LIG_SH3_3 | 194 | 200 | PF00018 | 0.262 |
| LIG_SH3_3 | 213 | 219 | PF00018 | 0.420 |
| LIG_SH3_3 | 262 | 268 | PF00018 | 0.214 |
| LIG_SH3_3 | 89 | 95 | PF00018 | 0.490 |
| LIG_SUMO_SIM_par_1 | 310 | 317 | PF11976 | 0.487 |
| LIG_SUMO_SIM_par_1 | 344 | 349 | PF11976 | 0.400 |
| LIG_SUMO_SIM_par_1 | 71 | 77 | PF11976 | 0.626 |
| LIG_TRAF2_1 | 272 | 275 | PF00917 | 0.446 |
| LIG_TYR_ITIM | 253 | 258 | PF00017 | 0.286 |
| MOD_CK1_1 | 12 | 18 | PF00069 | 0.754 |
| MOD_CK1_1 | 257 | 263 | PF00069 | 0.259 |
| MOD_CK1_1 | 277 | 283 | PF00069 | 0.249 |
| MOD_CK1_1 | 28 | 34 | PF00069 | 0.697 |
| MOD_CK1_1 | 293 | 299 | PF00069 | 0.228 |
| MOD_CK1_1 | 47 | 53 | PF00069 | 0.749 |
| MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.552 |
| MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.539 |
| MOD_GlcNHglycan | 273 | 279 | PF01048 | 0.612 |
| MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.285 |
| MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.236 |
| MOD_GSK3_1 | 25 | 32 | PF00069 | 0.636 |
| MOD_GSK3_1 | 290 | 297 | PF00069 | 0.342 |
| MOD_GSK3_1 | 342 | 349 | PF00069 | 0.480 |
| MOD_GSK3_1 | 68 | 75 | PF00069 | 0.635 |
| MOD_GSK3_1 | 8 | 15 | PF00069 | 0.735 |
| MOD_N-GLC_2 | 169 | 171 | PF02516 | 0.555 |
| MOD_NEK2_1 | 192 | 197 | PF00069 | 0.297 |
| MOD_NEK2_1 | 222 | 227 | PF00069 | 0.497 |
| MOD_NEK2_1 | 290 | 295 | PF00069 | 0.297 |
| MOD_NEK2_1 | 319 | 324 | PF00069 | 0.466 |
| MOD_PIKK_1 | 160 | 166 | PF00454 | 0.278 |
| MOD_PIKK_1 | 54 | 60 | PF00454 | 0.660 |
| MOD_PKA_2 | 222 | 228 | PF00069 | 0.441 |
| MOD_PKA_2 | 26 | 32 | PF00069 | 0.709 |
| MOD_PKA_2 | 319 | 325 | PF00069 | 0.496 |
| MOD_PKB_1 | 318 | 326 | PF00069 | 0.515 |
| MOD_Plk_1 | 25 | 31 | PF00069 | 0.612 |
| MOD_Plk_4 | 118 | 124 | PF00069 | 0.450 |
| MOD_Plk_4 | 145 | 151 | PF00069 | 0.279 |
| MOD_Plk_4 | 162 | 168 | PF00069 | 0.366 |
| MOD_Plk_4 | 243 | 249 | PF00069 | 0.328 |
| MOD_Plk_4 | 257 | 263 | PF00069 | 0.217 |
| MOD_Plk_4 | 69 | 75 | PF00069 | 0.656 |
| MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.279 |
| TRG_DiLeu_BaEn_2 | 235 | 241 | PF01217 | 0.418 |
| TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.323 |
| TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.521 |
| TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.250 |
| TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.238 |
| TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.602 |
| TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.403 |
| TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.520 |
| TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.667 |
| TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.366 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P222 | Leptomonas seymouri | 30% | 100% |
| A0A0N1P9L0 | Leptomonas seymouri | 72% | 100% |
| A0A0S4IU86 | Bodo saltans | 42% | 100% |
| A0A0S4IYL3 | Bodo saltans | 31% | 100% |
| A0A0S4IZ65 | Bodo saltans | 26% | 100% |
| A0A0S4IZG7 | Bodo saltans | 23% | 100% |
| A0A0S4J2G4 | Bodo saltans | 24% | 100% |
| A0A0S4JDA7 | Bodo saltans | 26% | 99% |
| A0A1X0NPW5 | Trypanosomatidae | 56% | 100% |
| A0A1X0P6F0 | Trypanosomatidae | 31% | 100% |
| A0A1X0P6P9 | Trypanosomatidae | 30% | 100% |
| A0A1X0P778 | Trypanosomatidae | 26% | 100% |
| A0A3Q8IB56 | Leishmania donovani | 29% | 100% |
| A0A3R7K844 | Trypanosoma rangeli | 32% | 100% |
| A0A3R7KEL4 | Trypanosoma rangeli | 56% | 100% |
| A0A3R7M893 | Trypanosoma rangeli | 27% | 100% |
| A0A3S5H5Y3 | Leishmania donovani | 95% | 100% |
| A1DI57 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 26% | 100% |
| A2A3V2 | Mus musculus | 24% | 100% |
| A2ASZ8 | Mus musculus | 25% | 78% |
| A2CEQ0 | Danio rerio | 26% | 78% |
| A2R5A0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 24% | 100% |
| A4H503 | Leishmania braziliensis | 85% | 100% |
| A4H8E6 | Leishmania braziliensis | 25% | 100% |
| A4H9X7 | Leishmania braziliensis | 30% | 100% |
| A4H9X8 | Leishmania braziliensis | 30% | 100% |
| A4HA67 | Leishmania braziliensis | 24% | 100% |
| A4HT75 | Leishmania infantum | 95% | 100% |
| A4HY43 | Leishmania infantum | 29% | 100% |
| A4RF23 | Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) | 25% | 100% |
| A5PJZ1 | Bos taurus | 25% | 76% |
| A6SL61 | Botryotinia fuckeliana (strain B05.10) | 24% | 100% |
| A7ER02 | Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) | 25% | 100% |
| B0G159 | Dictyostelium discoideum | 24% | 77% |
| B4F8I5 | Zea mays | 24% | 100% |
| B8ZHC9 | Rattus norvegicus | 26% | 100% |
| C9ZUP8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
| D0A0D8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
| E9AL65 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| E9ARX1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
| E9ARX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
| E9AS62 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
| F4HW79 | Arabidopsis thaliana | 22% | 100% |
| F4JU70 | Arabidopsis thaliana | 26% | 100% |
| G2QNH0 | Myceliophthora thermophila (strain ATCC 42464 / BCRC 31852 / DSM 1799) | 28% | 100% |
| K7VYZ9 | Zea mays | 28% | 100% |
| O04619 | Arabidopsis thaliana | 26% | 100% |
| O18757 | Oryctolagus cuniculus | 24% | 77% |
| O22342 | Gossypium hirsutum | 29% | 94% |
| O46373 | Oryctolagus cuniculus | 28% | 100% |
| O49447 | Arabidopsis thaliana | 29% | 96% |
| O65023 | Arabidopsis thaliana | 25% | 96% |
| O97470 | Dictyostelium discoideum | 28% | 100% |
| P02722 | Bos taurus | 28% | 100% |
| P02723 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 28% | 100% |
| P04709 | Zea mays | 29% | 94% |
| P04710 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
| P05141 | Homo sapiens | 29% | 100% |
| P12235 | Homo sapiens | 28% | 100% |
| P12236 | Homo sapiens | 26% | 100% |
| P12857 | Zea mays | 30% | 94% |
| P16260 | Homo sapiens | 23% | 100% |
| P16261 | Rattus norvegicus | 26% | 100% |
| P18238 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
| P18239 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
| P25083 | Solanum tuberosum | 29% | 94% |
| P27080 | Chlamydomonas reinhardtii | 31% | 100% |
| P27081 | Solanum tuberosum | 28% | 94% |
| P29518 | Zea mays | 24% | 83% |
| P31167 | Arabidopsis thaliana | 28% | 96% |
| P31691 | Oryza sativa subsp. japonica | 30% | 95% |
| P31692 | Parachlorella kessleri | 28% | 100% |
| P32007 | Bos taurus | 27% | 100% |
| P40941 | Arabidopsis thaliana | 30% | 95% |
| P48962 | Mus musculus | 27% | 100% |
| P49382 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 29% | 100% |
| P51881 | Mus musculus | 29% | 100% |
| Q000K2 | Tachyglossus aculeatus aculeatus | 29% | 100% |
| Q01888 | Bos taurus | 25% | 100% |
| Q05962 | Rattus norvegicus | 28% | 100% |
| Q05AQ3 | Xenopus tropicalis | 27% | 100% |
| Q09073 | Rattus norvegicus | 29% | 100% |
| Q09188 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
| Q0CEN9 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 24% | 100% |
| Q0P483 | Danio rerio | 27% | 100% |
| Q0UUH1 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 26% | 100% |
| Q0V7M4 | Bos taurus | 28% | 78% |
| Q19529 | Caenorhabditis elegans | 26% | 69% |
| Q1E7P0 | Coccidioides immitis (strain RS) | 24% | 100% |
| Q1ECW7 | Danio rerio | 21% | 100% |
| Q26365 | Drosophila melanogaster | 28% | 100% |
| Q27238 | Anopheles gambiae | 27% | 100% |
| Q29RM1 | Bos taurus | 23% | 100% |
| Q2UCW8 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 24% | 100% |
| Q2YDD9 | Bos taurus | 28% | 100% |
| Q3V132 | Mus musculus | 28% | 100% |
| Q41629 | Triticum aestivum | 30% | 100% |
| Q41630 | Triticum aestivum | 30% | 100% |
| Q4QDK0 | Leishmania major | 27% | 100% |
| Q4R8M0 | Macaca fascicularis | 28% | 100% |
| Q4X022 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 27% | 100% |
| Q54DU1 | Dictyostelium discoideum | 24% | 100% |
| Q54MZ4 | Dictyostelium discoideum | 25% | 84% |
| Q5AVW1 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 25% | 100% |
| Q5IS35 | Macaca fascicularis | 23% | 100% |
| Q5NVC1 | Pongo abelii | 23% | 100% |
| Q5PQ27 | Xenopus laevis | 27% | 100% |
| Q5R5A1 | Pongo abelii | 30% | 100% |
| Q5U3V7 | Danio rerio | 22% | 100% |
| Q5XH95 | Xenopus tropicalis | 25% | 71% |
| Q5XHA0 | Xenopus tropicalis | 26% | 77% |
| Q628Z2 | Caenorhabditis briggsae | 27% | 68% |
| Q66L49 | Danio rerio | 29% | 76% |
| Q6DG32 | Danio rerio | 26% | 100% |
| Q6GQS1 | Mus musculus | 25% | 78% |
| Q6KCM7 | Homo sapiens | 25% | 78% |
| Q6NUK1 | Homo sapiens | 25% | 76% |
| Q6NYZ6 | Danio rerio | 26% | 78% |
| Q6QRN9 | Sus scrofa | 26% | 100% |
| Q7PQV7 | Anopheles gambiae | 28% | 100% |
| Q7S2H8 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 29% | 100% |
| Q7T0U6 | Xenopus laevis | 26% | 77% |
| Q7ZY36 | Xenopus laevis | 25% | 77% |
| Q7ZYD5 | Xenopus laevis | 24% | 71% |
| Q86VD7 | Homo sapiens | 25% | 100% |
| Q8BMD8 | Mus musculus | 25% | 77% |
| Q8BVN7 | Mus musculus | 27% | 100% |
| Q8C0K5 | Mus musculus | 25% | 100% |
| Q8K3P6 | Rattus norvegicus | 25% | 78% |
| Q8LB08 | Arabidopsis thaliana | 26% | 100% |
| Q8N5S1 | Homo sapiens | 24% | 98% |
| Q8RXZ9 | Arabidopsis thaliana | 25% | 100% |
| Q8SQH5 | Bos taurus | 29% | 100% |
| Q8WUT9 | Homo sapiens | 24% | 100% |
| Q922G0 | Mus musculus | 26% | 100% |
| Q96CQ1 | Homo sapiens | 26% | 100% |
| Q9BV35 | Homo sapiens | 26% | 78% |
| Q9DAM5 | Mus musculus | 23% | 100% |
| Q9FI43 | Arabidopsis thaliana | 26% | 75% |
| Q9FI73 | Arabidopsis thaliana | 24% | 100% |
| Q9FLS8 | Arabidopsis thaliana | 27% | 76% |
| Q9FM86 | Arabidopsis thaliana | 27% | 100% |
| Q9H0C2 | Homo sapiens | 29% | 100% |
| Q9HC21 | Homo sapiens | 23% | 100% |
| Q9LY28 | Arabidopsis thaliana | 28% | 76% |
| Q9M024 | Arabidopsis thaliana | 26% | 88% |
| Q9SUV1 | Arabidopsis thaliana | 27% | 93% |
| V5BTC0 | Trypanosoma cruzi | 55% | 100% |
| V5BWX9 | Trypanosoma cruzi | 31% | 100% |