Align L-lactate dehydrogenase iron-sulfur cluster-binding protein LldF (characterized, see rationale)
to candidate Dsui_1583 Dsui_1583 (4Fe-4S) cluster-containing protein
Query= uniprot:Q8EGS5 (464 letters) >FitnessBrowser__PS:Dsui_1583 Length = 470 Score = 309 bits (791), Expect = 1e-88 Identities = 173/449 (38%), Positives = 258/449 (57%), Gaps = 20/449 (4%) Query: 34 KALWLLREK----RDRAAGSLPEWEQLRQLGSEIKLHTLTNLAQYLETFEQNCLANGIKV 89 KAL L++ K R AA ++E LR G +I+ L NL +LE FEQ G +V Sbjct: 23 KALKLVQVKFVPGRAAAAAEFGDFETLRDAGRDIRNRALENLDLWLERFEQEATRRGAQV 82 Query: 90 HWAKDGAEHNRIVHEILASHKVKKLVKSKSMLTEECHLNPYLEQRGIEVIDTDLGERIIQ 149 HWA+D AE N I+ I ++ VKK+VKSKSM++EEC LN LE G+ ++TDLGE I+Q Sbjct: 83 HWARDAAEANAIIVGIAQANGVKKVVKSKSMVSEECGLNDALEAAGVTPVETDLGEYILQ 142 Query: 150 L-AKMPPSHIVVPAIHMKKEEVGDLFHDKLGTKAGESDPLYLTRAARAHLREQFLSADAA 208 + PPSHIV P IH ++EV DLFH K G K D L R AR LR FLSAD Sbjct: 143 INDHEPPSHIVAPVIHKTRDEVSDLFHAKHG-KPRTEDIGALCREAREILRPHFLSADMG 201 Query: 209 MTGVNMAIADKGAVVVCTNEGNADMGANLPKLQLHSMGIDKVVPDIDSAAVLLRTLARNA 268 ++G N +A+ G+ V+ TNEGN + +P++ + GI+KVVP ++ +VLLR L R+A Sbjct: 202 ISGANFLVAETGSTVIVTNEGNGRLCTTVPRIHVALTGIEKVVPTLEDLSVLLRLLPRSA 261 Query: 269 TGQPVTTYSAFYRGPQVDG------EMHVIIVDNGRTEMMKDKILAESLKCIRCGGCLNT 322 TGQP+T Y + G G + H++++DNGR+ ++ + L E L+CIRCG C+N Sbjct: 262 TGQPITNYVSMNTGVAGSGDSDGPEQFHIVLLDNGRSRVLGSE-LKEMLRCIRCGACMNH 320 Query: 323 CPVYRRSGGYSYNYTIPGPIGIAVGATH---DNTNSIAWACTLCGSCTYVCPTKVPLDKI 379 CPVY+ GG++Y + PGP+G + ++ ++ + + T CG C+ VCP ++PL ++ Sbjct: 321 CPVYQAVGGHAYGWVYPGPMGSVLTPSYAGMEHAHELPHTATGCGQCSAVCPVRIPLPEL 380 Query: 380 IHHHRRLKAEAGKLPYGKNAYMPLVGKFMASTTLLNCSMGAARTALRILPGS--LLK--P 435 + R ++ EAG P+ + + L G + + L A L+ L G+ L+ P Sbjct: 381 MRKEREMQVEAGLRPWQERLSLKLWGWSASQSWLYGIGTAIAARFLKRLGGADQLIHRLP 440 Query: 436 FSGAWGKYRELPVAPNSSFEAWFKKHRSL 464 G W R+ P +F ++ ++L Sbjct: 441 LGGGWTDGRDFPAPAGKTFRELYRARKNL 469 Lambda K H 0.320 0.134 0.413 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: 565 Number of extensions: 37 Number of successful extensions: 7 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: 464 Length of database: 470 Length adjustment: 33 Effective length of query: 431 Effective length of database: 437 Effective search space: 188347 Effective search space used: 188347 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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