GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Desulfovibrio vulgaris Hildenborough

Align High-affinity branched-chain amino acid transport system permease protein BraD, component of Branched chain amino acid uptake transporter. Transports alanine (characterized)
to candidate 209487 DVU0548 high-affinity branched-chain amino acid ABC transporter, permease protein

Query= TCDB::P21627
         (307 letters)



>MicrobesOnline__882:209487
          Length = 302

 Score =  301 bits (771), Expect = 1e-86
 Identities = 156/302 (51%), Positives = 215/302 (71%), Gaps = 4/302 (1%)

Query: 6   HYLQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYIAFIAITLLAMMGL 65
           ++ + L  GLT GS YALIA+GYTMVYGII +INFAHGEVYMIG++ A I   +L + G 
Sbjct: 5   YFCELLFGGLTRGSIYALIALGYTMVYGIIELINFAHGEVYMIGAFTALIVAGVLGIYGF 64

Query: 66  DSVPLMMLAAFAASIIVTSAFGYSIERVAYRPLRGGNRLIPLISAIGMSIFLQNAVMLSQ 125
               ++++AA  A +I  +A+G+++E+VAY+PLR   RL PLISAIGMSIFLQN V+L+Q
Sbjct: 65  PEAGILIIAAIVA-VIYCAAYGFTLEKVAYKPLRDAPRLSPLISAIGMSIFLQNYVILAQ 123

Query: 126 DSKEKAIPTLLPGNFVFGESSMNGVVISYMQILIFVVTFLVMFGLTLFISRSRLGRACRA 185
            S     P L+P   +    +    +     +LI V + + M GLTLFI  +R+G+A RA
Sbjct: 124 TSDFVPFPRLVPDLAILEPIAH---ITGTSDVLIIVTSAITMVGLTLFIKYTRMGKAMRA 180

Query: 186 CAEDLKMTNLLGINSNNIIALTFVIGAALAAVAAVLLGMQYGVINPGIGFLAGIKAFTAA 245
            A++ KM  LLGI+++ +I+LTF+IG++LAA+  VL+    G +N  IGF+AGIKAFTAA
Sbjct: 181 TAQNRKMAMLLGIDADRVISLTFIIGSSLAAIGGVLIASHIGQVNFAIGFIAGIKAFTAA 240

Query: 246 VLGGIGSIPGAMLGGLLLGVAEAFGADVFGDQYKDVVAFGLLILVLLFRPTGILGRPEVE 305
           VLGGIGSIPGAM GGL+LG+ E+F        Y+D +AF LL+L+L+FRP+GILG+P+ +
Sbjct: 241 VLGGIGSIPGAMAGGLVLGLCESFATGYVSSDYEDALAFALLVLILIFRPSGILGKPKTQ 300

Query: 306 KV 307
           KV
Sbjct: 301 KV 302


Lambda     K      H
   0.328    0.145    0.413 

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: 339
Number of extensions: 18
Number of successful extensions: 6
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: 307
Length of database: 302
Length adjustment: 27
Effective length of query: 280
Effective length of database: 275
Effective search space:    77000
Effective search space used:    77000
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 48 (23.1 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