GapMind for catabolism of small carbon sources

 

Alignments for a candidate for L-LDH in Rhizobium johnstonii 3841

Align L-lactate dehydrogenase (cytochrome) (EC 1.1.2.3) (characterized)
to candidate WP_011653049.1 RL_RS18435 alpha-hydroxy acid oxidase

Query= reanno::Smeli:SM_b20850
         (378 letters)



>NCBI__GCF_000009265.1:WP_011653049.1
          Length = 380

 Score =  624 bits (1608), Expect = 0.0
 Identities = 305/376 (81%), Positives = 340/376 (90%)

Query: 1   MTQILEIRDLKALARRRVPKLFFDYADSGAWTEGTYRANEEDFAGIKLRQRVLVDMSDRS 60
           M   L I DLK LA+RRVPK+FFDYADSGAWTE TY ANE DF+ IKLRQRV+VDM++R+
Sbjct: 1   MAAPLTIADLKKLAQRRVPKMFFDYADSGAWTESTYAANESDFSQIKLRQRVMVDMTNRT 60

Query: 61  LETTMIGQKVSMPVALAPTGLTGMQHADGEMLAAQAAEAFGVPFTLSTMSICSIEDVASV 120
           LETTMIGQKVSMPVALAPTGLTGMQHADGEMLAA+AAE FGVPFTLSTMSICSIEDVAS 
Sbjct: 61  LETTMIGQKVSMPVALAPTGLTGMQHADGEMLAARAAEEFGVPFTLSTMSICSIEDVASA 120

Query: 121 TTKPFWFQLYVMREREFVLDLIDRAKAAKCSALVMTLDLQILGQRHKDLRNGLSAPPRLT 180
           TT+PFWFQLYVMR+++FVL+LI+RAKAA CSALV+T DLQILGQRHKDLRNGLSAPP+ T
Sbjct: 121 TTRPFWFQLYVMRDKDFVLNLINRAKAAGCSALVLTADLQILGQRHKDLRNGLSAPPKFT 180

Query: 181 PKHLWMMATRPGWCMKMLGTNRRTFRNIVGHAKSVADLSSLQAWTNEQFDPQLSWKDVEW 240
           PKH+W MATRP WC+ ML T RRTF NIVGHAK+V+ ++SL AWT+EQFDP+LSW DV W
Sbjct: 181 PKHVWQMATRPFWCLDMLQTKRRTFGNIVGHAKNVSSIASLSAWTHEQFDPRLSWADVAW 240

Query: 241 IKERWGGPLILKGILDPEDAKMAAKTGADAIIVSNHGGRQLDGAHSSISMLPRIVEAVGD 300
           IKE+WGGPLI+KGILDPEDA+ A  TGADAI+VSNHGGRQLDGA SSISMLP+IV+AVGD
Sbjct: 241 IKEQWGGPLIIKGILDPEDARAAVDTGADAIVVSNHGGRQLDGAPSSISMLPKIVDAVGD 300

Query: 301 QIEVHLDGGIRSGQDVLKAIALGAKGTYIGRPFLYGLGALGKEGVTLALDIIRKEMDTTM 360
           +IEVHLDGGIRSGQDVLKA+ALGAKGTYIGRPFLYGLGA+GKEGV+LAL IIRKEMD TM
Sbjct: 301 RIEVHLDGGIRSGQDVLKAVALGAKGTYIGRPFLYGLGAMGKEGVSLALGIIRKEMDITM 360

Query: 361 ALCGKRRITEVGRDII 376
           ALCGKR I +V   II
Sbjct: 361 ALCGKRDINDVNSSII 376


Lambda     K      H
   0.321    0.136    0.406 

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: 545
Number of extensions: 17
Number of successful extensions: 1
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: 378
Length of database: 380
Length adjustment: 30
Effective length of query: 348
Effective length of database: 350
Effective search space:   121800
Effective search space used:   121800
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 (21.9 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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