GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcvT in Sinorhizobium meliloti 1021

Align Aminomethyltransferase; EC 2.1.2.10; Glycine cleavage system T protein (uncharacterized)
to candidate SMc01662 SMc01662 oxidoreductase

Query= curated2:A4J2F6
         (364 letters)



>FitnessBrowser__Smeli:SMc01662
          Length = 815

 Score =  169 bits (427), Expect = 3e-46
 Identities = 114/344 (33%), Positives = 176/344 (51%), Gaps = 11/344 (3%)

Query: 26  WLMPVQYEGIIAEHQAVRSAAGLFDVSHMGEIQISGPTAREFVQRLVTNDISRLKPGCAI 85
           W     +E    EH AVRS  GLFD++  G+I++ G  A+ F+QRL  N+++ + PG  +
Sbjct: 465 WKRQNWFENQREEHLAVRSGVGLFDMTSFGKIRVEGRDAQAFLQRLCANEMN-VDPGRVV 523

Query: 86  YSPMCNPQGGTVDDLLVYQLEDQQYLLVVNASNTDKDFHWIVSQ-QVPGVEIQNVSEVTC 144
           Y+ M N +GG   DL V +L    + LVV  +   +D  W+    +   V I +V+    
Sbjct: 524 YTQMLNARGGIESDLTVTRLSQTAFFLVVPGATLQRDLAWLRKHVRDEFVVITDVTAAES 583

Query: 145 QLALQGPQAEKILQRLTAVDLSHIKSFCFVYGAVE---GIHCLISRTGYTGEAGFELYFP 201
            L + GP+A +++Q+++  D S+          +E   G+     R  Y GE G+ELY  
Sbjct: 584 VLCVMGPRARELMQKVSPNDFSNEAHPFATAREIEIGMGL-ARAHRVTYVGELGWELYVS 642

Query: 202 ASHAERVWQAIMATGATDGLRPVGLGARDTLRFEACLALYGHELTDDISPLMAGLGWTVK 261
              A  V++ +   GA  GL+  GL   D+ R E     +GH++TD+   L AGLG+ VK
Sbjct: 643 TDQAAHVFETLELAGADVGLKLCGLHTLDSCRIEKAFRHFGHDITDEDHVLEAGLGFAVK 702

Query: 262 FNKPEFVGKEPLLKQKEAGTTYQLVGLEMID-RGIPRQGYAIFKEGQEVGWITSGTFAPT 320
             K EF+G+E +L +++ G + +LV   + D   +     AI ++G+ VG ITSG +   
Sbjct: 703 PGKGEFIGREAVLAKRDNGLSRRLVQFRLSDPEPLLFHNEAIVRDGEIVGTITSGNYGHH 762

Query: 321 LGKNMGLGYVEI---PFADV-GKELNIMVRNKPLKARIVKKPFY 360
           LG  +GLGYV       ADV      I +    +KA    KP Y
Sbjct: 763 LGGAIGLGYVACKGESDADVLASAYEIEIAGTRVKAEASLKPMY 806


Lambda     K      H
   0.321    0.138    0.418 

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: 686
Number of extensions: 50
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 364
Length of database: 815
Length adjustment: 35
Effective length of query: 329
Effective length of database: 780
Effective search space:   256620
Effective search space used:   256620
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 (21.8 bits)
S2: 52 (24.6 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