GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Azospirillum brasilense Sp245

Align L-threonine 3-dehydrogenase (EC 1.1.1.103) (characterized)
to candidate AZOBR_RS16515 AZOBR_RS16515 S-(hydroxymethyl)glutathione dehydrogenase

Query= BRENDA::Q5JI69
         (350 letters)



>FitnessBrowser__azobra:AZOBR_RS16515
          Length = 372

 Score =  112 bits (280), Expect = 2e-29
 Identities = 111/361 (30%), Positives = 170/361 (47%), Gaps = 52/361 (14%)

Query: 18  ELVEVDVPKPGPGEVLIKVLATSICGTDLHIYEWNEWAQSRIKPPQIMGHEVAGEVVEVG 77
           E+ EV+V  P  GEVL++++AT +C TD +     +   S    P I+GHE AG V EVG
Sbjct: 17  EIEEVEVAAPRQGEVLVRIVATGVCHTDAYTLSGMD---SEGVFPAILGHEGAGIVEEVG 73

Query: 78  PGVEDLQVGDYISVETHIVCGKCYACKHNRYHVCQ---NTKIFGVDMDG----------- 123
           PGV  +QVGD++       CGKC  C   + ++CQ    T+  G+  DG           
Sbjct: 74  PGVTSVQVGDHVIPLYTPECGKCKFCLSGKTNLCQAIRATQGKGLMPDGTSRFTAKGQPV 133

Query: 124 -------VFAHYAIVPAKNAWKNPKDMPPEYAALQEPLGNAVDTVL------AGPIAGRS 170
                   F+ Y ++P     K  K  P E   L   LG  V T +      A    G +
Sbjct: 134 FHYMGTSTFSEYTVLPEIAVAKINKAAPLEKVCL---LGCGVTTGMGAVRNTAKVEPGST 190

Query: 171 TLITGAGPLGL---LGIAVAKASGAYPVIVSEPSEFRRKLAKKVGADYVVNPFEED-PVK 226
             I G G +GL   +G  +AKAS    + ++ P +F  ++AK++GA  VVNP + D P++
Sbjct: 191 VAIFGLGGIGLSAIIGAVMAKASRIIGIDIN-PDKF--EIAKQLGATDVVNPKDYDRPIQ 247

Query: 227 FVM-DITDGAGVEVFLEFSGAPKALEQGLKAVTPG-GRVSLLGL--FPREVTIDFNNLI- 281
            V+ ++TDG GV+   E  G  K +   L+    G G   ++G+     E++     L+ 
Sbjct: 248 EVLVEMTDG-GVDYSFECIGNVKVMRAALECCHKGWGESVIIGVAGAGEEISTRPFQLVT 306

Query: 282 --IFKALEVHGITGRHLWETWYTVSSLIQSGKLNLDPIITHKYKGFDKFEEAFELMRAGK 339
             +++     G+ GR     +         G+  LD  ITH   G +   +AF+LM  GK
Sbjct: 307 GRVWRGSAFGGVRGRSELPDYV---ERYLKGEFELDTFITHT-MGLEDINKAFDLMHEGK 362

Query: 340 T 340
           +
Sbjct: 363 S 363


Lambda     K      H
   0.319    0.139    0.423 

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: 29
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: 350
Length of database: 372
Length adjustment: 29
Effective length of query: 321
Effective length of database: 343
Effective search space:   110103
Effective search space used:   110103
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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