GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Microvirga lotononidis WSM3557

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate WP_009763936.1 MICLODRAFT_RS21540 NAD(P)-dependent alcohol dehydrogenase

Query= curated2:Q67N85
         (351 letters)



>NCBI__GCF_000262405.1:WP_009763936.1
          Length = 357

 Score =  128 bits (322), Expect = 2e-34
 Identities = 116/363 (31%), Positives = 166/363 (45%), Gaps = 29/363 (7%)

Query: 5   MRALRKLEAGPGATLQEVPIPTIGPRDVLVKVRAASICGTDYHIYTWDPWSAGRVKPPLT 64
           MRA   +E G    L E PIP IGP D LV++   +ICGTD HI   +      V P LT
Sbjct: 4   MRAAIFVEPGR-IVLDEKPIPNIGPLDALVRISTTTICGTDIHILKGEY----PVAPGLT 58

Query: 65  IGHELAGEVVAVGREVTACKVGDYVSAETHIVCNRCPRCHMGEYHLC-ENTKI------- 116
           IGHE  G +  +G  V   + G  V A           C  G +      TK        
Sbjct: 59  IGHEPVGIIEKLGSAVQGYREGQRVIAGAITPSGYSEACLCGCHSQDGAGTKHGWKAMGG 118

Query: 117 --LGVDTDGAFAEYVAVPEQNIWVNDKDIPFELQSIQEPL-GNAVHTALNGDLTAR---- 169
              G   DG  AEY+ VP+     N   +P  L   Q  +  + + T  +G  + R    
Sbjct: 119 WKFGNTIDGCQAEYLRVPDA--MANLAPVPDGLTDEQVLMCPDILSTGFSGAESGRIRIG 176

Query: 170 -SVLITGCGPIGIMSVPVAKMAGAEIVMAMDINEYRLQLAGQLGADVLINPTKQDPVEVV 228
            +V +   GPIG+ +   AK+ GA  ++A++    R+ ++ ++GAD +I+ TK DPVE +
Sbjct: 177 DTVAVFAQGPIGLCATAGAKLMGATTIIAVESLPERIDMSRRMGADHVIDFTKADPVEEI 236

Query: 229 RSYTRGYGADVVLEMSGNPTAIRQGLKAARNGARISLLGLPGRPLELDLAADVIMRGLVL 288
           R  T G G DV +E  G        L+  R G  +S LG+    L + L  D  + GL  
Sbjct: 237 RRLTDGRGVDVSIEALGRQQTFEAALRVLRPGGTLSSLGVYSGDLRIPL--DGFLAGLGD 294

Query: 289 QGITGRRMWQTWYQVRSLYRAGLAERL--RPLVTHRMPLEQIDAAMELMGSGQSG--KIV 344
             I          ++R L  A  + R+  RPLVTHR  L+QI+ A +L    + G  K+ 
Sbjct: 295 YTIRTTLCPGGKERMRRLISAIASGRVDTRPLVTHRFKLDQIEEAYDLFSHQRDGVLKVA 354

Query: 345 LVP 347
           + P
Sbjct: 355 IAP 357


Lambda     K      H
   0.320    0.137    0.415 

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: 344
Number of extensions: 24
Number of successful extensions: 4
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: 351
Length of database: 357
Length adjustment: 29
Effective length of query: 322
Effective length of database: 328
Effective search space:   105616
Effective search space used:   105616
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 2021. 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