Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate N515DRAFT_1250 N515DRAFT_1250 L-lactate dehydrogenase (cytochrome)
Query= reanno::acidovorax_3H11:Ac3H11_1623 (390 letters) >lcl|FitnessBrowser__Dyella79:N515DRAFT_1250 N515DRAFT_1250 L-lactate dehydrogenase (cytochrome) Length = 379 Score = 444 bits (1142), Expect = e-129 Identities = 222/377 (58%), Positives = 278/377 (73%), Gaps = 4/377 (1%) Query: 7 ITCIEDLRAIAQRRVPRMFYDYADSGSYTEGTYRANESDFQRIKLRQRVAVNMEGRSTRT 66 IT + DLR +A+RRVPR F++YAD G+Y E T R N + + IK RQRV +N++ RS T Sbjct: 5 ITNVLDLRELARRRVPRAFFEYADRGAYDEVTLRGNRAALESIKFRQRVMMNVDQRSLAT 64 Query: 67 TMVGQDVAMPVAIAPTGLTGMQHADGEILGAKAAKAFGIPFTLSTMSICSIEDIAEHTGR 126 ++VGQ ++MP+AIAPTGLTG+QH GEILGA+AA GIPF LST+SICSIE + + + Sbjct: 65 SVVGQPISMPLAIAPTGLTGLQHGAGEILGARAATKAGIPFCLSTVSICSIEQVRDAV-Q 123 Query: 127 HPFWFQVYVMRDRDFIERLIDRAKAANCSALQLTLDLQILGQRHKDIKNGLSAPPKPTIA 186 PFWFQ+YVMRDR F LI RA A CSAL LT DL + GQRH++IKNGLS PPK T+ Sbjct: 124 APFWFQLYVMRDRGFARDLIRRASDAGCSALMLTADLTVQGQRHREIKNGLSVPPKITLR 183 Query: 187 NLINLATKPRWCLGMLGTKRRSFGNIVGHAKGVGDLSSLSSWTAEQFDPQLNWGDVEWIK 246 NL ++ +KPRW ML RSFGN+ G +G L++L+ W A QFDP LNW D+EWI+ Sbjct: 184 NLFDVMSKPRWAWSMLRAPSRSFGNLAGRIQGTDSLTTLAQWIANQFDPTLNWQDLEWIR 243 Query: 247 KRWGGKLILKGIMDAEDARLAVNSGADALIVSNHGGRQLDGAPSSIAALPGIADAVAQMG 306 + W GKLILKGIMD EDARLA G DA++VSNHGGRQLDGAP+SI LP IADAV G Sbjct: 244 ELWPGKLILKGIMDEEDARLAAAHGVDAIVVSNHGGRQLDGAPASIEVLPRIADAV---G 300 Query: 307 GGIEVWMDGGIRSGQDVLKARALGAQGTLIGRSFLYGLGAYGEAGVTRALQIIQKELDIT 366 ++V DGGI SGQDVLKA ALGA+ LIG++FLYGLGA GE GV R ++II++EL ++ Sbjct: 301 DKLDVLFDGGILSGQDVLKALALGARAGLIGKAFLYGLGALGEDGVARTIEIIRRELSVS 360 Query: 367 MAFCGHTNINTVDRSIL 383 MA G T++ + R +L Sbjct: 361 MALTGQTDVRRIGRDVL 377 Lambda K H 0.320 0.137 0.412 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: 424 Number of extensions: 15 Number of successful extensions: 3 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: 390 Length of database: 379 Length adjustment: 30 Effective length of query: 360 Effective length of database: 349 Effective search space: 125640 Effective search space used: 125640 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: 50 (23.9 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 preprint 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