GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Paenisporosarcina indica PN2

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 WP_075617863.1 GY23_RS03805 branched-chain amino acid ABC transporter permease

Query= TCDB::P21627
         (307 letters)



>NCBI__GCF_001939075.1:WP_075617863.1
          Length = 286

 Score =  129 bits (324), Expect = 8e-35
 Identities = 85/289 (29%), Positives = 148/289 (51%), Gaps = 18/289 (6%)

Query: 12  VNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSY--IAFIAITLLAMMGLDSVP 69
           +NGL  G    L+A G T+++G++ ++NFAHG ++  G+Y  + F A+T       DS  
Sbjct: 9   INGLATGMLIFLLAAGLTLIFGLMDVLNFAHGGLFAWGAYSSVWFYALT-------DSFV 61

Query: 70  LMMLAAFAASIIVTSAFGYSIERVAYRPLRGGNRLIPLISAIGMSIFLQNAVMLSQDSKE 129
           L +L A    +I+    G+  E++  +P+ G N +  ++  +G  + L   + +     +
Sbjct: 62  LAILGAILTGVIL----GFITEKLIIKPVYG-NHVQQILITLGFMLVLTEMLKVVFGPNQ 116

Query: 130 KAIPTLLPGNFVFGESSMNGVVISYMQILIFVVTFLVMFGLTLFISRSRLGRACRACAED 189
            A+ T  P N V G   +  V+I   ++ I +V FLV       + ++++G   RA   +
Sbjct: 117 IAVRT--PENLV-GSWEIGDVIIIKYRVFIIIVGFLVFGIFQYILKKTKIGLIVRAGVLN 173

Query: 190 LKMTNLLGINSNNIIALTFVIGAALAAVAAVLLGMQYGVINPGIGFLAGIKAFTAAVLGG 249
            +M   LGIN  N+    F+ GA+LAA+   L     GVI   +G    I  F   V+GG
Sbjct: 174 KEMVQTLGINIKNVFLYVFIAGASLAAIGGALFAPYSGVIYAEMGMEYAILGFIVVVIGG 233

Query: 250 IGSIPGAMLGGLLLGVAEAFGADVFGDQYKDVVAFGLLILVLLFRPTGI 298
           +GS PG++L  +L+G+  ++ A  +       V   ++ +VL+FRP G+
Sbjct: 234 MGSFPGSLLAAILVGLVGSYMA-YYVPSLSLAVNMIIMAIVLIFRPQGL 281


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: 300
Number of extensions: 19
Number of successful extensions: 3
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: 286
Length adjustment: 26
Effective length of query: 281
Effective length of database: 260
Effective search space:    73060
Effective search space used:    73060
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 24 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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