GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aguA in Synechococcus elongatus PCC 7942

Align agmatine deiminase (EC 3.5.3.12) (characterized)
to candidate Synpcc7942_2402 Synpcc7942_2402 hypothetical protein

Query= BRENDA::Q9PAQ3
         (363 letters)



>FitnessBrowser__SynE:Synpcc7942_2402
          Length = 376

 Score =  333 bits (854), Expect = 4e-96
 Identities = 167/342 (48%), Positives = 226/342 (66%), Gaps = 7/342 (2%)

Query: 24  RFPAEWEPQSAILIAWPHANTDWSAHLADVEETYIALVAAITRFQMVIICVLDDDLQTYT 83
           RFPAEWE Q  +LIAWPHA++DW + L  V+  Y  L  A+TRF+ ++I   + D     
Sbjct: 38  RFPAEWEAQDGVLIAWPHADSDWRSLLDQVDRVYRDLAEAVTRFEQLLIVTPEPDR---V 94

Query: 84  EARLRSASVAMQQVRFTVASYNDTWLRDSGPITLIGTNRDFRLLDFRFTGWGGKFEAKAD 143
             +L   +    +++      NDTW RD GP+T + T    RLLD+ F GWG KF A  D
Sbjct: 95  AEQLAQTTANCDRIQIVELPTNDTWSRDFGPLT-VETPAGLRLLDWGFNGWGLKFAANHD 153

Query: 144 DQLVSVLHANGLFKNTQMHSINFALEGGAIETDGAGTLLTTWRCLHE--RHPQRTRKTLD 201
           +Q+   L   G+F  T + ++    EGG+IE+DG GTLLTT +CL E  R+P  +R+ + 
Sbjct: 154 NQVTRRLWQQGIFGTTPLETVPLIFEGGSIESDGRGTLLTTSQCLLEANRNPGLSREAIA 213

Query: 202 ANLTAWLAQNRVLWLEHGYLEGDDTDAHIDTLARFASTDSIVYQSCDNTTDSHYAELQAM 261
             +   L  +R+LWLEHG+LEGDDTDAHIDTL R A  D+++Y +CD+ +DSH AEL A+
Sbjct: 214 QIIQRQLGGDRLLWLEHGHLEGDDTDAHIDTLVRIAPNDTLIYVACDDPSDSHAAELTAL 273

Query: 262 ANELTALRTTEGRAYRLFPLPWTKPILDQD-RRLPASYANFLIIEGAVLMPTYDDPADTI 320
             EL ALR  +G+ Y L PLPW +P  D D +RLP +YAN+L+I GAVL+PTY+DPAD  
Sbjct: 274 EAELKALRAADGQPYHLIPLPWPQPCFDADGQRLPTTYANYLVINGAVLVPTYNDPADEA 333

Query: 321 AQSVLAEAFPTREIVPVPCRPLIWQNGSLHCITMQIPAGLLA 362
           A + +A AFP R  + + CRPL+ Q+GSLHCITMQ+PAGLL+
Sbjct: 334 AIAAIAAAFPDRLAIGINCRPLLEQHGSLHCITMQLPAGLLS 375


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: 497
Number of extensions: 21
Number of successful extensions: 5
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: 376
Length adjustment: 30
Effective length of query: 333
Effective length of database: 346
Effective search space:   115218
Effective search space used:   115218
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 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