GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dadA in Herbaspirillum seropedicae SmR1

Align D-arginine dehydrogenase (EC 1.4.99.6) (characterized)
to candidate HSERO_RS11185 HSERO_RS11185 amino acid dehydrogenase

Query= BRENDA::Q9HTQ0
         (432 letters)



>FitnessBrowser__HerbieS:HSERO_RS11185
          Length = 423

 Score =  226 bits (576), Expect = 1e-63
 Identities = 146/417 (35%), Positives = 215/417 (51%), Gaps = 14/417 (3%)

Query: 2   RVLVLGSGVIGTASAYYLARAGFEVVVVDRQDGPALETSFANAGQVSPGYASPWAAPGIP 61
           ++ V+G G+ G  SAY+LA  G+EV V++R+   A E +F ++G ++PG A P   PG  
Sbjct: 7   QIAVIGGGLSGICSAYFLATKGYEVAVIERRAHVAEEATFGDSGLLAPGTAMPLTLPGA- 65

Query: 62  LKAMKWLLEKHAPLAIKLTSDPSQYAWMLQMLRNCTAERYAVNKERMVRLSEYSRDCLDE 121
           L       +    + +   +D  +  WM +  R      +A +K  + RLS Y +D   +
Sbjct: 66  LATFACRFQDEPRVLLASGADFGRRRWM-RATRAAQQHHFAQHKLILSRLSAYGQDLTQQ 124

Query: 122 LRAETGIAYEGRTLGTTQLFRTQAQLDAAGKDIAVLERSGVPYE--VLDRDGIARVEPAL 179
           L+A   + +E  + G   LFR  A+  AA         S   Y+   LD  GI  +EPA 
Sbjct: 125 LQAHYNMEHEN-SAGVFHLFRQSAE--AARLPALQEAASQCEYKQLTLDAAGIRALEPAF 181

Query: 180 AKVADKLVGALRLPNDQTGDCQLFTTRLAEMAKGLGVEFRFGQNIE--RLDFAGDRINGV 237
           +  A  L GAL  P+D  G+  LF  ++   A+ LGV F F   +   R +F G R+   
Sbjct: 182 SSEA-ALAGALYYPDDIAGNSVLFAKQMRNAAQALGVSFHFNSTVSSIRSEFGG-RVTLE 239

Query: 238 LVNGEL---LTADHYVLALGSYSPQLLKPLGIKAPVYPLKGYSLTVPITNPEMAPTSTIL 294
           + +  L   LT D  V+A G  S  LL+PL    P+  L+ YS  VP+ NP+ APT  + 
Sbjct: 240 VQSPHLASHLTMDAVVVAAGMASAALLQPLDTSLPLRALQSYSALVPVKNPDDAPTMALY 299

Query: 295 DETYKVAITRFDQRIRVGGMAEIAGFDLSLNPRRRETLEMITTDLYPEGGDISQATFWTG 354
           D++YKVA+TR   RIR+ G+        +L P+    L  I  D YP   + +QA FW+ 
Sbjct: 300 DDSYKVAMTRLGSRIRISGLLGFVPASQTLPPKALRNLLKIAGDYYPNAANYNQAHFWSN 359

Query: 355 LRPATPDGTPIVGATRYRNLFLNTGHGTLGWTMACGSGRYLADLMAKKRPQISTEGL 411
                P G P+VG TR  N+F+N GHG  GW  + GS R L+D+MA +  +I+T GL
Sbjct: 360 SIAMMPTGLPVVGPTRQGNIFVNVGHGVTGWAASVGSARLLSDMMAGEETEIATAGL 416


Lambda     K      H
   0.318    0.135    0.401 

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: 366
Number of extensions: 16
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: 432
Length of database: 423
Length adjustment: 32
Effective length of query: 400
Effective length of database: 391
Effective search space:   156400
Effective search space used:   156400
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 51 (24.3 bits)

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

Links

Downloads

Related tools

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