GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aguA in Stenotrophomonas chelatiphaga DSM 21508

Align agmatine deiminase (EC 3.5.3.12) (characterized)
to candidate WP_057506685.1 ABB28_RS00175 agmatine deiminase family protein

Query= BRENDA::Q9PAQ3
         (363 letters)



>NCBI__GCF_001431535.1:WP_057506685.1
          Length = 346

 Score =  507 bits (1306), Expect = e-148
 Identities = 244/339 (71%), Positives = 277/339 (81%)

Query: 24  RFPAEWEPQSAILIAWPHANTDWSAHLADVEETYIALVAAITRFQMVIICVLDDDLQTYT 83
           RFPAEWE QS +LIAWP A+TDW+  L  VEETYIALVAAITRFQ V+ICV DDD++TY 
Sbjct: 6   RFPAEWEAQSGVLIAWPTADTDWADRLGQVEETYIALVAAITRFQPVLICVADDDVETYA 65

Query: 84  EARLRSASVAMQQVRFTVASYNDTWLRDSGPITLIGTNRDFRLLDFRFTGWGGKFEAKAD 143
           E RLRS  + MQ+VRF  A+Y+DTWLRDSGPITL   +  F+LLDFRFTGWGGKF+A  D
Sbjct: 66  EMRLRSNRIDMQRVRFVTAAYDDTWLRDSGPITLQRKDGGFQLLDFRFTGWGGKFDATLD 125

Query: 144 DQLVSVLHANGLFKNTQMHSINFALEGGAIETDGAGTLLTTWRCLHERHPQRTRKTLDAN 203
           DQLV VL A  +F +  + SI FALEGG IETDG GTLLTTW+CLHERHP R R +L A+
Sbjct: 126 DQLVGVLDAARVFNDAPVRSIAFALEGGGIETDGQGTLLTTWKCLHERHPDRDRASLSAD 185

Query: 204 LTAWLAQNRVLWLEHGYLEGDDTDAHIDTLARFASTDSIVYQSCDNTTDSHYAELQAMAN 263
           L  WL Q+RVLWL+HGYLEGDDTDAHIDTLARFAS DSIVYQ+CD+ +DSH+AELQAM  
Sbjct: 186 LADWLQQDRVLWLDHGYLEGDDTDAHIDTLARFASADSIVYQACDDASDSHHAELQAMGA 245

Query: 264 ELTALRTTEGRAYRLFPLPWTKPILDQDRRLPASYANFLIIEGAVLMPTYDDPADTIAQS 323
           EL ALRT +G+ YRLFPLPW +P+LD+ RRL ASYANFLI+ GAVLMP Y D AD  A+ 
Sbjct: 246 ELAALRTADGQPYRLFPLPWPQPVLDEGRRLAASYANFLIVNGAVLMPAYGDAADEAARD 305

Query: 324 VLAEAFPTREIVPVPCRPLIWQNGSLHCITMQIPAGLLA 362
           VLA AFP REIV VPCR LIWQNGSLHCITMQ+PAGLLA
Sbjct: 306 VLAAAFPDREIVQVPCRSLIWQNGSLHCITMQLPAGLLA 344


Lambda     K      H
   0.322    0.134    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: 551
Number of extensions: 18
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: 363
Length of database: 346
Length adjustment: 29
Effective length of query: 334
Effective length of database: 317
Effective search space:   105878
Effective search space used:   105878
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: 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