GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aguA in Synechococcus elongatus PCC 7942

Align Putative agmatine deiminase; EC 3.5.3.12; Agmatine iminohydrolase (uncharacterized)
to candidate Synpcc7942_2461 Synpcc7942_2461 hypothetical protein

Query= curated2:A6VVD9
         (369 letters)



>FitnessBrowser__SynE:Synpcc7942_2461
          Length = 477

 Score =  168 bits (426), Expect = 2e-46
 Identities = 121/395 (30%), Positives = 191/395 (48%), Gaps = 56/395 (14%)

Query: 14  FRMPAEHEPQEQVWMAWPTREDNWREKGKHAQAEFVAVATAIAQSTKVTFIVDAKHYEQA 73
           FRMPAE EP   +WMA+PT E+   + G  +Q    A+  AIA + K+ F+++    +  
Sbjct: 65  FRMPAEFEPITSIWMAYPTYEN---QAGYPSQTVQKAMVKAIAPTVKIDFLLNEPEEKVI 121

Query: 74  ------RLALP-DQIRVIEIPSDDCWMRDIGATYVVNDQGERRANSWQFNAWGGELDGLY 126
                    +P  Q+R   +P +D W+RD+G  + VN   + +   + FNAW   L    
Sbjct: 122 INGWLKTAGIPASQVRYHLVPHEDLWIRDMGPIFAVNAD-QTQVVDFGFNAWS-YLAATD 179

Query: 127 DSWEQDNAVAEKMAAVTGDYVYHAPLILEGGSIHVDGEGTLYTTEECLLHPSRNPHLSKE 186
            +   D  V  K+A      +  + LI EGG+   +G+GTL  TE   L   RNP L+KE
Sbjct: 180 PAAMTDEQVDRKVAGDLDLPILRSSLISEGGNREFNGKGTLMLTEAVELQ--RNPGLTKE 237

Query: 187 DIEDLLKVYLNVEKIIWLKDGLYNDE----------------TNGHVDNIMHVIRPGVVA 230
            IE  LK   N++K+IWL++G+ +DE                T GH+D     +    + 
Sbjct: 238 KIETELKRVFNLKKVIWLQEGVIDDELSYRGKLPDGSLTVLATGGHIDEYARFVDSNTIL 297

Query: 231 LTDC---EDSNDPQYAIS----KAAIKVLSQAIDAKGRTLEIIKLPMPGPLFVS---EDE 280
           L +    E ++DP  AI+    +  +K+L  A D  G+   I+++P   P++V+   ED 
Sbjct: 298 LAEVTAEERASDPLAAINYQRLEENLKILQAATDQDGKPFRIVRIPAAKPIYVNMTKEDA 357

Query: 281 AKNLLKSDSM--------NRQVGERLAASYANFLITNNSIVFPTFG--------EKTDEQ 324
               L+  +         + Q+   LAASY NF+I N+ ++ P +         ++ D+ 
Sbjct: 358 VFQALQELTFEDGTVIQDDDQIKTILAASYLNFVIANDVVIVPRYWQPDRNLEYQQKDQA 417

Query: 325 AKEILQKAFPEHKVIGVYARNILLGGGNIHCITQQ 359
           A    Q  FP  K++ +   NI  GGG +HCI QQ
Sbjct: 418 ALAAFQSVFPNKKIVAINPENINAGGGGMHCIVQQ 452


Lambda     K      H
   0.316    0.134    0.402 

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: 436
Number of extensions: 28
Number of successful extensions: 7
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: 369
Length of database: 477
Length adjustment: 32
Effective length of query: 337
Effective length of database: 445
Effective search space:   149965
Effective search space used:   149965
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 (21.6 bits)
S2: 50 (23.9 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