A family of very long coiled-coil proteins, likely performing cytoskeletal functions.. Two varieties have evolved, one with an N-terminal FYVE domain (Non-TM) and another with a C-terminal PDZ domain (might be TM)
Lipid Metabolism, Uncharacterized
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. | yes | yes: 20 |
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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005576 | extracellular region | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0000795 | synaptonemal complex | 3 | 1 |
GO:0099086 | synaptonemal structure | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HRT8
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0006810 | transport | 3 | 5 |
GO:0006869 | lipid transport | 5 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0019538 | protein metabolic process | 3 | 5 |
GO:0042157 | lipoprotein metabolic process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0051179 | localization | 1 | 5 |
GO:0051234 | establishment of localization | 2 | 5 |
GO:0071702 | organic substance transport | 4 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007130 | synaptonemal complex assembly | 4 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0070192 | chromosome organization involved in meiotic cell cycle | 3 | 1 |
GO:0070193 | synaptonemal complex organization | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0008289 | lipid binding | 2 | 5 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 5 |
GO:0046872 | metal ion binding | 4 | 5 |
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0003774 | cytoskeletal motor activity | 1 | 1 |
GO:0003777 | microtubule motor activity | 2 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005524 | ATP binding | 5 | 1 |
GO:0008017 | microtubule binding | 5 | 1 |
GO:0008092 | cytoskeletal protein binding | 3 | 1 |
GO:0015631 | tubulin binding | 4 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0030554 | adenyl nucleotide binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 1 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 1506 | 1510 | PF00656 | 0.192 |
CLV_C14_Caspase3-7 | 1588 | 1592 | PF00656 | 0.393 |
CLV_C14_Caspase3-7 | 1733 | 1737 | PF00656 | 0.425 |
CLV_C14_Caspase3-7 | 2139 | 2143 | PF00656 | 0.435 |
CLV_NRD_NRD_1 | 1469 | 1471 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 1595 | 1597 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 1750 | 1752 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 1878 | 1880 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 1904 | 1906 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 1983 | 1985 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 2109 | 2111 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 2128 | 2130 | PF00675 | 0.381 |
CLV_PCSK_KEX2_1 | 1469 | 1471 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 1595 | 1597 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 1750 | 1752 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 1878 | 1880 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 1904 | 1906 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 1983 | 1985 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 2109 | 2111 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 2128 | 2130 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 1026 | 1030 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 1065 | 1069 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 1104 | 1108 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 1143 | 1147 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 1182 | 1186 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 1221 | 1225 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 1260 | 1264 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 1299 | 1303 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 1338 | 1342 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 1377 | 1381 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 1416 | 1420 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 1470 | 1474 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 1720 | 1724 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 1925 | 1929 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 2048 | 2052 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 2095 | 2099 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 714 | 718 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 792 | 796 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 831 | 835 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 870 | 874 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 909 | 913 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 948 | 952 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 987 | 991 | PF00082 | 0.392 |
CLV_Separin_Metazoa | 2016 | 2020 | PF03568 | 0.594 |
DEG_APCC_DBOX_1 | 1639 | 1647 | PF00400 | 0.369 |
DEG_APCC_DBOX_1 | 2094 | 2102 | PF00400 | 0.390 |
DEG_SCF_FBW7_1 | 98 | 105 | PF00400 | 0.531 |
DEG_SIAH_1 | 125 | 133 | PF03145 | 0.506 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.544 |
DOC_ANK_TNKS_1 | 1850 | 1857 | PF00023 | 0.484 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.504 |
DOC_CKS1_1 | 1969 | 1974 | PF01111 | 0.592 |
DOC_MAPK_gen_1 | 1844 | 1852 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 1921 | 1930 | PF00069 | 0.472 |
DOC_MAPK_gen_1 | 2128 | 2134 | PF00069 | 0.335 |
DOC_MIT_MIM_1 | 1638 | 1646 | PF04212 | 0.409 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 1472 | 1476 | PF00917 | 0.182 |
DOC_USP7_MATH_1 | 1495 | 1499 | PF00917 | 0.192 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.232 |
DOC_USP7_MATH_1 | 1804 | 1808 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 1814 | 1818 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 1887 | 1891 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 1900 | 1904 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.258 |
DOC_USP7_MATH_1 | 1989 | 1993 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 2003 | 2007 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.458 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 1968 | 1973 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 1978 | 1983 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 2008 | 2013 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.491 |
LIG_14-3-3_CanoR_1 | 1695 | 1705 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 1720 | 1725 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 1789 | 1798 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 1801 | 1808 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 1878 | 1886 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 1951 | 1959 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 2039 | 2047 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 2073 | 2080 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 2084 | 2091 | PF00244 | 0.345 |
LIG_Actin_WH2_2 | 1774 | 1791 | PF00022 | 0.441 |
LIG_APCC_ABBA_1 | 1537 | 1542 | PF00400 | 0.415 |
LIG_APCC_ABBA_1 | 1703 | 1708 | PF00400 | 0.413 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.538 |
LIG_Clathr_ClatBox_1 | 1815 | 1819 | PF01394 | 0.499 |
LIG_CtBP_PxDLS_1 | 1856 | 1862 | PF00389 | 0.473 |
LIG_FHA_1 | 1698 | 1704 | PF00498 | 0.425 |
LIG_FHA_1 | 1953 | 1959 | PF00498 | 0.554 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.246 |
LIG_FHA_1 | 2080 | 2086 | PF00498 | 0.508 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.352 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.507 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.245 |
LIG_FHA_2 | 1993 | 1999 | PF00498 | 0.529 |
LIG_FHA_2 | 2028 | 2034 | PF00498 | 0.550 |
LIG_LIR_Gen_1 | 2049 | 2056 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 2044 | 2050 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 2125 | 2130 | PF02991 | 0.389 |
LIG_REV1ctd_RIR_1 | 32 | 42 | PF16727 | 0.270 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.282 |
LIG_SH2_SRC | 2052 | 2055 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 2052 | 2056 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 2070 | 2073 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.592 |
LIG_SH3_1 | 104 | 110 | PF00018 | 0.556 |
LIG_SH3_1 | 1983 | 1989 | PF00018 | 0.535 |
LIG_SH3_2 | 2014 | 2019 | PF14604 | 0.582 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.570 |
LIG_SH3_3 | 1894 | 1900 | PF00018 | 0.515 |
LIG_SH3_3 | 1966 | 1972 | PF00018 | 0.592 |
LIG_SH3_3 | 1983 | 1989 | PF00018 | 0.501 |
LIG_SH3_3 | 2011 | 2017 | PF00018 | 0.597 |
LIG_SUMO_SIM_par_1 | 1813 | 1819 | PF11976 | 0.496 |
LIG_SxIP_EBH_1 | 51 | 65 | PF03271 | 0.282 |
LIG_TRAF2_1 | 1670 | 1673 | PF00917 | 0.437 |
LIG_TRAF2_1 | 1710 | 1713 | PF00917 | 0.416 |
LIG_TRAF2_1 | 189 | 192 | PF00917 | 0.230 |
LIG_TRAF2_1 | 2100 | 2103 | PF00917 | 0.382 |
LIG_TRAF2_1 | 2118 | 2121 | PF00917 | 0.322 |
LIG_TYR_ITIM | 2050 | 2055 | PF00017 | 0.404 |
LIG_WW_3 | 2016 | 2020 | PF00397 | 0.585 |
MOD_CDK_SPK_2 | 1978 | 1983 | PF00069 | 0.551 |
MOD_CDK_SPxK_1 | 1978 | 1984 | PF00069 | 0.593 |
MOD_CDK_SPxK_1 | 98 | 104 | PF00069 | 0.557 |
MOD_CDK_SPxxK_3 | 2008 | 2015 | PF00069 | 0.610 |
MOD_CK1_1 | 1803 | 1809 | PF00069 | 0.518 |
MOD_CK1_1 | 1890 | 1896 | PF00069 | 0.502 |
MOD_CK1_1 | 1992 | 1998 | PF00069 | 0.546 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.253 |
MOD_CK2_1 | 1472 | 1478 | PF00069 | 0.186 |
MOD_CK2_1 | 1547 | 1553 | PF00069 | 0.402 |
MOD_CK2_1 | 1696 | 1702 | PF00069 | 0.408 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.264 |
MOD_CK2_1 | 1878 | 1884 | PF00069 | 0.547 |
MOD_CK2_1 | 1992 | 1998 | PF00069 | 0.532 |
MOD_CK2_1 | 2027 | 2033 | PF00069 | 0.581 |
MOD_GlcNHglycan | 1658 | 1661 | PF01048 | 0.370 |
MOD_GlcNHglycan | 1742 | 1745 | PF01048 | 0.482 |
MOD_GlcNHglycan | 1802 | 1805 | PF01048 | 0.515 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.282 |
MOD_GlcNHglycan | 1812 | 1815 | PF01048 | 0.513 |
MOD_GlcNHglycan | 1821 | 1824 | PF01048 | 0.529 |
MOD_GlcNHglycan | 1991 | 1994 | PF01048 | 0.572 |
MOD_GlcNHglycan | 2000 | 2003 | PF01048 | 0.521 |
MOD_GlcNHglycan | 2006 | 2009 | PF01048 | 0.542 |
MOD_GlcNHglycan | 2075 | 2078 | PF01048 | 0.567 |
MOD_GlcNHglycan | 2085 | 2088 | PF01048 | 0.396 |
MOD_GlcNHglycan | 2134 | 2137 | PF01048 | 0.356 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.533 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.609 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.541 |
MOD_GSK3_1 | 1740 | 1747 | PF00069 | 0.465 |
MOD_GSK3_1 | 1789 | 1796 | PF00069 | 0.475 |
MOD_GSK3_1 | 1800 | 1807 | PF00069 | 0.457 |
MOD_GSK3_1 | 1810 | 1817 | PF00069 | 0.517 |
MOD_GSK3_1 | 1887 | 1894 | PF00069 | 0.501 |
MOD_GSK3_1 | 1953 | 1960 | PF00069 | 0.554 |
MOD_GSK3_1 | 1964 | 1971 | PF00069 | 0.566 |
MOD_GSK3_1 | 2004 | 2011 | PF00069 | 0.589 |
MOD_GSK3_1 | 2029 | 2036 | PF00069 | 0.526 |
MOD_GSK3_1 | 2079 | 2086 | PF00069 | 0.515 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.713 |
MOD_N-GLC_2 | 1719 | 1721 | PF02516 | 0.375 |
MOD_NEK2_1 | 1802 | 1807 | PF00069 | 0.521 |
MOD_NEK2_1 | 2085 | 2090 | PF00069 | 0.368 |
MOD_NEK2_1 | 2105 | 2110 | PF00069 | 0.445 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.447 |
MOD_PIKK_1 | 1067 | 1073 | PF00454 | 0.228 |
MOD_PIKK_1 | 1106 | 1112 | PF00454 | 0.214 |
MOD_PIKK_1 | 111 | 117 | PF00454 | 0.538 |
MOD_PIKK_1 | 1223 | 1229 | PF00454 | 0.228 |
MOD_PIKK_1 | 1340 | 1346 | PF00454 | 0.228 |
MOD_PIKK_1 | 1457 | 1463 | PF00454 | 0.214 |
MOD_PIKK_1 | 1557 | 1563 | PF00454 | 0.355 |
MOD_PIKK_1 | 1891 | 1897 | PF00454 | 0.557 |
MOD_PIKK_1 | 2033 | 2039 | PF00454 | 0.495 |
MOD_PIKK_1 | 2079 | 2085 | PF00454 | 0.474 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.214 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.214 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.214 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.242 |
MOD_PIKK_1 | 482 | 488 | PF00454 | 0.228 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.228 |
MOD_PIKK_1 | 716 | 722 | PF00454 | 0.228 |
MOD_PIKK_1 | 794 | 800 | PF00454 | 0.242 |
MOD_PIKK_1 | 833 | 839 | PF00454 | 0.256 |
MOD_PIKK_1 | 950 | 956 | PF00454 | 0.214 |
MOD_PIKK_1 | 989 | 995 | PF00454 | 0.242 |
MOD_PKA_1 | 1878 | 1884 | PF00069 | 0.530 |
MOD_PKA_2 | 1483 | 1489 | PF00069 | 0.186 |
MOD_PKA_2 | 1800 | 1806 | PF00069 | 0.526 |
MOD_PKA_2 | 1877 | 1883 | PF00069 | 0.536 |
MOD_PKA_2 | 1998 | 2004 | PF00069 | 0.509 |
MOD_PKA_2 | 2038 | 2044 | PF00069 | 0.467 |
MOD_PKA_2 | 2072 | 2078 | PF00069 | 0.489 |
MOD_PKA_2 | 2083 | 2089 | PF00069 | 0.377 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.516 |
MOD_Plk_1 | 1547 | 1553 | PF00069 | 0.383 |
MOD_Plk_1 | 1650 | 1656 | PF00069 | 0.399 |
MOD_Plk_1 | 1891 | 1897 | PF00069 | 0.522 |
MOD_Plk_1 | 2120 | 2126 | PF00069 | 0.365 |
MOD_Plk_2-3 | 1547 | 1553 | PF00069 | 0.383 |
MOD_Plk_4 | 1483 | 1489 | PF00069 | 0.186 |
MOD_Plk_4 | 1794 | 1800 | PF00069 | 0.488 |
MOD_Plk_4 | 1953 | 1959 | PF00069 | 0.570 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.376 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.555 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.531 |
MOD_ProDKin_1 | 1968 | 1974 | PF00069 | 0.594 |
MOD_ProDKin_1 | 1978 | 1984 | PF00069 | 0.547 |
MOD_ProDKin_1 | 2008 | 2014 | PF00069 | 0.609 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.522 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.503 |
MOD_SUMO_for_1 | 1544 | 1547 | PF00179 | 0.406 |
MOD_SUMO_rev_2 | 1437 | 1447 | PF00179 | 0.211 |
MOD_SUMO_rev_2 | 1623 | 1627 | PF00179 | 0.424 |
TRG_DiLeu_BaEn_1 | 1848 | 1853 | PF01217 | 0.472 |
TRG_DiLeu_BaEn_4 | 1450 | 1456 | PF01217 | 0.186 |
TRG_DiLeu_BaEn_4 | 1553 | 1559 | PF01217 | 0.389 |
TRG_DiLeu_BaEn_4 | 192 | 198 | PF01217 | 0.284 |
TRG_DiLeu_LyEn_5 | 1848 | 1853 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 1706 | 1709 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 2047 | 2050 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 2052 | 2055 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.279 |
TRG_ER_diArg_1 | 1469 | 1471 | PF00400 | 0.186 |
TRG_ER_diArg_1 | 1639 | 1642 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 1692 | 1695 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 1749 | 1751 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 1862 | 1865 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 1904 | 1906 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 1982 | 1984 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 2018 | 2021 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 2109 | 2111 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 2127 | 2129 | PF00400 | 0.380 |
TRG_NES_CRM1_1 | 1617 | 1630 | PF08389 | 0.395 |
TRG_NES_CRM1_1 | 1848 | 1861 | PF08389 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 1469 | 1474 | PF00026 | 0.186 |
TRG_Pf-PMV_PEXEL_1 | 1707 | 1712 | PF00026 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 1751 | 1755 | PF00026 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 1851 | 1855 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 1864 | 1868 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 2099 | 2103 | PF00026 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H530 | Leishmania donovani | 98% | 100% |
A4H3J9 | Leishmania braziliensis | 61% | 100% |
A4H7R4 | Leishmania braziliensis | 25% | 99% |
E9ACH4 | Leishmania major | 83% | 100% |