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)
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: 15 |
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: 4 |
NetGPI | no | yes: 0, no: 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005576 | extracellular region | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0006810 | transport | 3 | 4 |
GO:0006869 | lipid transport | 5 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0019538 | protein metabolic process | 3 | 4 |
GO:0042157 | lipoprotein metabolic process | 4 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0051179 | localization | 1 | 4 |
GO:0051234 | establishment of localization | 2 | 4 |
GO:0071702 | organic substance transport | 4 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 5 |
GO:0008289 | lipid binding | 2 | 4 |
GO:0043167 | ion binding | 2 | 5 |
GO:0043169 | cation binding | 3 | 4 |
GO:0046872 | metal ion binding | 4 | 4 |
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 | 1826 | 1830 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 1948 | 1952 | PF00656 | 0.593 |
CLV_NRD_NRD_1 | 1833 | 1835 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 2092 | 2094 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 2108 | 2110 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 2339 | 2341 | PF00675 | 0.405 |
CLV_PCSK_KEX2_1 | 1833 | 1835 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 2092 | 2094 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 2108 | 2110 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 2339 | 2341 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 2259 | 2263 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 2306 | 2310 | PF00082 | 0.483 |
CLV_Separin_Metazoa | 2227 | 2231 | PF03568 | 0.582 |
DEG_APCC_DBOX_1 | 2305 | 2313 | PF00400 | 0.487 |
DEG_SCF_FBW7_1 | 98 | 105 | PF00400 | 0.535 |
DEG_SPOP_SBC_1 | 93 | 97 | PF00917 | 0.489 |
DOC_ANK_TNKS_1 | 1115 | 1122 | PF00023 | 0.257 |
DOC_ANK_TNKS_1 | 1232 | 1239 | PF00023 | 0.257 |
DOC_ANK_TNKS_1 | 1522 | 1529 | PF00023 | 0.257 |
DOC_ANK_TNKS_1 | 1600 | 1607 | PF00023 | 0.257 |
DOC_ANK_TNKS_1 | 1717 | 1724 | PF00023 | 0.268 |
DOC_ANK_TNKS_1 | 2064 | 2071 | PF00023 | 0.477 |
DOC_ANK_TNKS_1 | 301 | 308 | PF00023 | 0.257 |
DOC_ANK_TNKS_1 | 485 | 492 | PF00023 | 0.257 |
DOC_CKS1_1 | 1 | 6 | PF01111 | 0.475 |
DOC_CKS1_1 | 2180 | 2185 | PF01111 | 0.660 |
DOC_CKS1_1 | 2291 | 2296 | PF01111 | 0.507 |
DOC_MAPK_gen_1 | 2058 | 2066 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 2132 | 2141 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 1748 | 1755 | PF00069 | 0.257 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 1911 | 1915 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.236 |
DOC_USP7_MATH_1 | 1990 | 1994 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 2018 | 2022 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 2111 | 2115 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 2214 | 2218 | PF00917 | 0.550 |
DOC_USP7_UBL2_3 | 1864 | 1868 | PF12436 | 0.438 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 2179 | 2184 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 2189 | 2194 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 2219 | 2224 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 2290 | 2295 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.456 |
LIG_14-3-3_CanoR_1 | 1910 | 1920 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 1935 | 1940 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 2003 | 2008 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 2092 | 2100 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 2162 | 2170 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 2250 | 2258 | PF00244 | 0.492 |
LIG_Actin_WH2_2 | 1988 | 2005 | PF00022 | 0.501 |
LIG_APCC_ABBA_1 | 1776 | 1781 | PF00400 | 0.292 |
LIG_APCC_ABBA_1 | 1918 | 1923 | PF00400 | 0.533 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.490 |
LIG_CtBP_PxDLS_1 | 2070 | 2076 | PF00389 | 0.477 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.589 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.488 |
LIG_FHA_1 | 1913 | 1919 | PF00498 | 0.517 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.292 |
LIG_FHA_1 | 2164 | 2170 | PF00498 | 0.524 |
LIG_FHA_1 | 2291 | 2297 | PF00498 | 0.553 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.346 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.283 |
LIG_FHA_2 | 1780 | 1786 | PF00498 | 0.257 |
LIG_FHA_2 | 187 | 193 | PF00498 | 0.304 |
LIG_FHA_2 | 1935 | 1941 | PF00498 | 0.488 |
LIG_FHA_2 | 2239 | 2245 | PF00498 | 0.553 |
LIG_Integrin_isoDGR_2 | 1952 | 1954 | PF01839 | 0.537 |
LIG_LIR_Gen_1 | 2260 | 2267 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 2255 | 2261 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 2336 | 2341 | PF02991 | 0.432 |
LIG_MYND_1 | 115 | 119 | PF01753 | 0.547 |
LIG_PCNA_yPIPBox_3 | 1864 | 1876 | PF02747 | 0.450 |
LIG_PDZ_Class_1 | 2349 | 2354 | PF00595 | 0.367 |
LIG_REV1ctd_RIR_1 | 32 | 42 | PF16727 | 0.316 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.333 |
LIG_SH2_SRC | 2263 | 2266 | PF00017 | 0.461 |
LIG_SH2_SRC | 2281 | 2284 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 2156 | 2160 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 2263 | 2267 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 2281 | 2284 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.517 |
LIG_SH3_1 | 104 | 110 | PF00018 | 0.576 |
LIG_SH3_2 | 2225 | 2230 | PF14604 | 0.579 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.666 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.551 |
LIG_SH3_3 | 2177 | 2183 | PF00018 | 0.643 |
LIG_SH3_3 | 2222 | 2228 | PF00018 | 0.578 |
LIG_SH3_3 | 2291 | 2297 | PF00018 | 0.501 |
LIG_SxIP_EBH_1 | 51 | 65 | PF03271 | 0.333 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.459 |
LIG_TRAF2_1 | 1782 | 1785 | PF00917 | 0.257 |
LIG_TRAF2_1 | 1888 | 1891 | PF00917 | 0.522 |
LIG_TRAF2_1 | 190 | 193 | PF00917 | 0.302 |
LIG_TRAF2_1 | 1925 | 1928 | PF00917 | 0.508 |
LIG_TRAF2_1 | 1983 | 1986 | PF00917 | 0.483 |
LIG_TRAF2_1 | 2311 | 2314 | PF00917 | 0.479 |
LIG_TRAF2_1 | 2329 | 2332 | PF00917 | 0.401 |
LIG_TYR_ITIM | 2261 | 2266 | PF00017 | 0.459 |
LIG_Vh1_VBS_1 | 1817 | 1835 | PF01044 | 0.266 |
LIG_WW_3 | 2227 | 2231 | PF00397 | 0.582 |
MOD_CDK_SPK_2 | 2290 | 2295 | PF00069 | 0.511 |
MOD_CDK_SPxK_1 | 2189 | 2195 | PF00069 | 0.620 |
MOD_CDK_SPxK_1 | 98 | 104 | PF00069 | 0.530 |
MOD_CDK_SPxxK_3 | 111 | 118 | PF00069 | 0.545 |
MOD_CDK_SPxxK_3 | 2219 | 2226 | PF00069 | 0.584 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.479 |
MOD_CK1_1 | 1945 | 1951 | PF00069 | 0.533 |
MOD_CK1_1 | 2011 | 2017 | PF00069 | 0.508 |
MOD_CK1_1 | 2200 | 2206 | PF00069 | 0.493 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.331 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.679 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.495 |
MOD_CK2_1 | 1779 | 1785 | PF00069 | 0.302 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.571 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.327 |
MOD_CK2_1 | 1911 | 1917 | PF00069 | 0.526 |
MOD_CK2_1 | 1934 | 1940 | PF00069 | 0.500 |
MOD_CK2_1 | 2092 | 2098 | PF00069 | 0.554 |
MOD_CK2_1 | 2238 | 2244 | PF00069 | 0.570 |
MOD_GlcNHglycan | 1805 | 1809 | PF01048 | 0.266 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.586 |
MOD_GlcNHglycan | 1957 | 1960 | PF01048 | 0.622 |
MOD_GlcNHglycan | 2016 | 2019 | PF01048 | 0.530 |
MOD_GlcNHglycan | 2020 | 2023 | PF01048 | 0.501 |
MOD_GlcNHglycan | 2026 | 2029 | PF01048 | 0.492 |
MOD_GlcNHglycan | 2035 | 2038 | PF01048 | 0.477 |
MOD_GlcNHglycan | 2217 | 2220 | PF01048 | 0.564 |
MOD_GlcNHglycan | 2286 | 2289 | PF01048 | 0.543 |
MOD_GlcNHglycan | 2298 | 2301 | PF01048 | 0.413 |
MOD_GlcNHglycan | 2345 | 2348 | PF01048 | 0.395 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.442 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.626 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.512 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.558 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.417 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.282 |
MOD_GSK3_1 | 1955 | 1962 | PF00069 | 0.617 |
MOD_GSK3_1 | 2003 | 2010 | PF00069 | 0.490 |
MOD_GSK3_1 | 2014 | 2021 | PF00069 | 0.474 |
MOD_GSK3_1 | 2164 | 2171 | PF00069 | 0.525 |
MOD_GSK3_1 | 2175 | 2182 | PF00069 | 0.575 |
MOD_GSK3_1 | 2215 | 2222 | PF00069 | 0.567 |
MOD_GSK3_1 | 2240 | 2247 | PF00069 | 0.542 |
MOD_GSK3_1 | 2296 | 2303 | PF00069 | 0.475 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.545 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.266 |
MOD_N-GLC_2 | 1934 | 1936 | PF02516 | 0.516 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.699 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.298 |
MOD_NEK2_1 | 2016 | 2021 | PF00069 | 0.525 |
MOD_NEK2_1 | 2316 | 2321 | PF00069 | 0.442 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.372 |
MOD_PIKK_1 | 1023 | 1029 | PF00454 | 0.283 |
MOD_PIKK_1 | 1062 | 1068 | PF00454 | 0.299 |
MOD_PIKK_1 | 1101 | 1107 | PF00454 | 0.283 |
MOD_PIKK_1 | 1140 | 1146 | PF00454 | 0.283 |
MOD_PIKK_1 | 1179 | 1185 | PF00454 | 0.316 |
MOD_PIKK_1 | 1218 | 1224 | PF00454 | 0.266 |
MOD_PIKK_1 | 1257 | 1263 | PF00454 | 0.316 |
MOD_PIKK_1 | 1296 | 1302 | PF00454 | 0.299 |
MOD_PIKK_1 | 1324 | 1330 | PF00454 | 0.266 |
MOD_PIKK_1 | 1363 | 1369 | PF00454 | 0.266 |
MOD_PIKK_1 | 1402 | 1408 | PF00454 | 0.266 |
MOD_PIKK_1 | 1430 | 1436 | PF00454 | 0.266 |
MOD_PIKK_1 | 1469 | 1475 | PF00454 | 0.283 |
MOD_PIKK_1 | 1508 | 1514 | PF00454 | 0.266 |
MOD_PIKK_1 | 1547 | 1553 | PF00454 | 0.283 |
MOD_PIKK_1 | 1586 | 1592 | PF00454 | 0.283 |
MOD_PIKK_1 | 1625 | 1631 | PF00454 | 0.316 |
MOD_PIKK_1 | 1664 | 1670 | PF00454 | 0.316 |
MOD_PIKK_1 | 1703 | 1709 | PF00454 | 0.316 |
MOD_PIKK_1 | 1742 | 1748 | PF00454 | 0.283 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.299 |
MOD_PIKK_1 | 2102 | 2108 | PF00454 | 0.608 |
MOD_PIKK_1 | 2244 | 2250 | PF00454 | 0.541 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.283 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.283 |
MOD_PIKK_1 | 326 | 332 | PF00454 | 0.266 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.290 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.266 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.276 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.324 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.302 |
MOD_PIKK_1 | 538 | 544 | PF00454 | 0.266 |
MOD_PIKK_1 | 577 | 583 | PF00454 | 0.283 |
MOD_PIKK_1 | 605 | 611 | PF00454 | 0.266 |
MOD_PIKK_1 | 644 | 650 | PF00454 | 0.299 |
MOD_PIKK_1 | 683 | 689 | PF00454 | 0.266 |
MOD_PIKK_1 | 722 | 728 | PF00454 | 0.277 |
MOD_PIKK_1 | 761 | 767 | PF00454 | 0.277 |
MOD_PIKK_1 | 800 | 806 | PF00454 | 0.316 |
MOD_PIKK_1 | 839 | 845 | PF00454 | 0.266 |
MOD_PIKK_1 | 878 | 884 | PF00454 | 0.333 |
MOD_PIKK_1 | 906 | 912 | PF00454 | 0.283 |
MOD_PIKK_1 | 945 | 951 | PF00454 | 0.327 |
MOD_PIKK_1 | 984 | 990 | PF00454 | 0.316 |
MOD_PK_1 | 2003 | 2009 | PF00069 | 0.421 |
MOD_PKA_1 | 2092 | 2098 | PF00069 | 0.538 |
MOD_PKA_2 | 1779 | 1785 | PF00069 | 0.266 |
MOD_PKA_2 | 1934 | 1940 | PF00069 | 0.486 |
MOD_PKA_2 | 2014 | 2020 | PF00069 | 0.530 |
MOD_PKA_2 | 2091 | 2097 | PF00069 | 0.526 |
MOD_PKA_2 | 2249 | 2255 | PF00069 | 0.530 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.465 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.295 |
MOD_Plk_1 | 2174 | 2180 | PF00069 | 0.565 |
MOD_Plk_1 | 2244 | 2250 | PF00069 | 0.491 |
MOD_Plk_1 | 2331 | 2337 | PF00069 | 0.453 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.266 |
MOD_Plk_2-3 | 2175 | 2181 | PF00069 | 0.572 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.575 |
MOD_Plk_4 | 2008 | 2014 | PF00069 | 0.512 |
MOD_Plk_4 | 2164 | 2170 | PF00069 | 0.519 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.333 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.584 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.556 |
MOD_ProDKin_1 | 2179 | 2185 | PF00069 | 0.656 |
MOD_ProDKin_1 | 2189 | 2195 | PF00069 | 0.570 |
MOD_ProDKin_1 | 2219 | 2225 | PF00069 | 0.585 |
MOD_ProDKin_1 | 2290 | 2296 | PF00069 | 0.508 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.478 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.460 |
MOD_SUMO_for_1 | 1789 | 1792 | PF00179 | 0.266 |
MOD_SUMO_for_1 | 190 | 193 | PF00179 | 0.266 |
MOD_SUMO_rev_2 | 1861 | 1866 | PF00179 | 0.519 |
TRG_DiLeu_BaEn_1 | 1754 | 1759 | PF01217 | 0.266 |
TRG_DiLeu_BaEn_1 | 2062 | 2067 | PF01217 | 0.472 |
TRG_DiLeu_BaEn_4 | 1784 | 1790 | PF01217 | 0.266 |
TRG_DiLeu_BaEn_4 | 1791 | 1797 | PF01217 | 0.315 |
TRG_DiLeu_BaEn_4 | 192 | 198 | PF01217 | 0.333 |
TRG_DiLeu_LyEn_5 | 2062 | 2067 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 1921 | 1924 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 2258 | 2261 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 2263 | 2266 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.316 |
TRG_ER_diArg_1 | 1907 | 1910 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 2029 | 2032 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 2076 | 2079 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 2107 | 2109 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 2229 | 2232 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 2338 | 2340 | PF00400 | 0.412 |
TRG_NES_CRM1_1 | 1855 | 1867 | PF08389 | 0.333 |
TRG_NES_CRM1_1 | 2062 | 2075 | PF08389 | 0.470 |
TRG_NES_CRM1_1 | 613 | 627 | PF08389 | 0.266 |
TRG_Pf-PMV_PEXEL_1 | 159 | 163 | PF00026 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 1922 | 1927 | PF00026 | 0.538 |
TRG_Pf-PMV_PEXEL_1 | 2065 | 2069 | PF00026 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 2082 | 2086 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 2310 | 2314 | PF00026 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H530 | Leishmania donovani | 79% | 100% |
A4HRT8 | Leishmania infantum | 83% | 100% |
A4HW58 | Leishmania infantum | 27% | 80% |