Align Dihydrolipoyllysine-residue (2-methylpropanoyl)transferase (EC 2.3.1.168) (characterized)
to candidate WP_073038431.1 BUB04_RS07775 2-oxoglutarate dehydrogenase complex dihydrolipoyllysine-residue succinyltransferase
Query= reanno::Smeli:SMc03203 (426 letters) >NCBI__GCF_900129305.1:WP_073038431.1 Length = 455 Score = 226 bits (577), Expect = 8e-64 Identities = 160/453 (35%), Positives = 226/453 (49%), Gaps = 38/453 (8%) Query: 6 IKMPDVGEGVAEAELVEWHVKPGDPVREDMVLAAVMTDKATVEIPSPVTGKVLWLGAEVG 65 I +PDVGE V EA L EW VKPG+ V + VL + TDK T+E+ + G V L E G Sbjct: 5 IVIPDVGESVQEAVLAEWFVKPGERVTKGTVLFVLETDKVTLEVAAESDGVVEIL-VEAG 63 Query: 66 DTVAVKAPLVRIETAGEAGEAAPDS------IPEALAEQVLDEPVAVSSRLEAKAPPQPE 119 +TV V + RI+T A EA P+ +P ++ E+ + + AP PE Sbjct: 64 ETVTVGTVVGRIDTEA-ASEAVPEKGAEASVVPASVGEEPEEGETLAAEVARVVAPKGPE 122 Query: 120 KPAPKPAP-APREAPDLSAK---PLASPAVRLRARESGIDLRQVAGTGPAGRITHEDLDL 175 + P+P P EAP + P P+V A E GIDL +VAGTGP GR+T DL L Sbjct: 123 EAEAVPSPEVPAEAPPSAGAAEMPQVFPSVARLAAEKGIDLSRVAGTGPYGRVTRGDLLL 182 Query: 176 FISRGAE------------PLPAQTG---------LVRKTAVEEVR--MIGLRRRIAEKM 212 F+ E P PA T R + E +R M +R+RIAE++ Sbjct: 183 FLESQTEEPTPKEVPVPQAPSPAPTAPPHAPPKPESPRDESPETIRKPMSRIRKRIAERL 242 Query: 213 SLSTSRIPHITYVEEVDMTALEDLRATMNRD-RKPEQAKLTILPFLMRALVKTVAEQPGV 271 + +T EVDM + D R R+ L I+ F ++A V + E P V Sbjct: 243 VHAKQTTAMLTTFNEVDMGRVMDFRRRFKESFREKYGVSLGIMSFFVKACVAALQEIPEV 302 Query: 272 NATFDDHAGVIHRHAAVHIGIATQTPAGLTVPVVRHAEARGIWDCAAELNRLADAARTGT 331 NA D V +RH VH+G+A GL VPV+R+A+ G + + R Sbjct: 303 NAFIDGDDIVYNRH--VHMGVAIGAERGLVVPVIRYADRLGFAEIEQAIVDFVKKVRENR 360 Query: 332 ATRDELTGSTITISSLGAIGGIASTPVINHPEVAIVGVNKIAVRPVWDGAQFVPRKIMNL 391 +L G T TIS+ G G + STP++N P+ I+G++KI RPV Q V R +M + Sbjct: 361 LQLSDLEGGTFTISNGGVYGSLLSTPILNPPQSGILGLHKIEDRPVVVDGQVVVRPMMYV 420 Query: 392 SSSFDHRVIDGWDAAVFVQRLKTLLETPALIFV 424 + S+DHR+IDG +A F++R+K +E P + V Sbjct: 421 ALSYDHRIIDGREAVTFLKRIKEFIEDPERLLV 453 Lambda K H 0.317 0.133 0.384 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 472 Number of extensions: 28 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 426 Length of database: 455 Length adjustment: 32 Effective length of query: 394 Effective length of database: 423 Effective search space: 166662 Effective search space used: 166662 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory