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_075619038.1 GY23_RS09730 branched-chain amino acid ABC transporter permease

Query= TCDB::P21627
         (307 letters)



>NCBI__GCF_001939075.1:WP_075619038.1
          Length = 294

 Score =  230 bits (587), Expect = 3e-65
 Identities = 125/302 (41%), Positives = 195/302 (64%), Gaps = 17/302 (5%)

Query: 8   LQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYIAFIAITLLAMMGLDS 67
           ++QL+NG+T+GS YA++A+G+T+V+G++G+IN AHGE++MIG   AFI +   +++GL  
Sbjct: 3   IEQLINGITLGSIYAIVALGFTLVFGVLGIINMAHGEIFMIG---AFIGVVTTSVLGL-- 57

Query: 68  VPLMMLAAFAASIIVTSAFGYSIERVAYRPLRGG---NRLIPLISAIGMSIFLQNAVMLS 124
            PL +  AF A+I VT+A GY +ER+A RPLRG    + L PLIS IG+SI L+N     
Sbjct: 58  -PLWI--AFIAAIGVTAALGYLLERIALRPLRGKQGVSHLAPLISTIGVSIILENLSHHL 114

Query: 125 QDSKEKAIPTLLPGNFVFGESSMNGVVISYMQILIFVVTFLVMFGLTLFISRSRLGRACR 184
             +  +         F   +  +  + +  +QILIFV++  +M  L+ ++S+++ G+A R
Sbjct: 115 FGAGNQPFRNA----FADIQFQIGSITVYLVQILIFVISIALMLTLSFWLSKTKAGKALR 170

Query: 185 ACAEDLKMTNLLGINSNNIIALTFVIGAALAAVAAVLLGMQYGVINPGIGFLAGIKAFTA 244
           A AE+L+  +LLG+N+   I  T +I +A+  +A +L+GM +  +NP +G   G+K    
Sbjct: 171 ATAENLETASLLGVNTKRTITTTVIIASAMGGIAGILVGMAFNSVNPQMGLSMGLKGLAI 230

Query: 245 AVLGGIGSIPGAMLGGLLLGVAEAFGADVFGDQ-YKDVVAFGLLILVLLFRPTGILGRPE 303
            +LGG+G++ GAM GGLLLGVAE  G   +GD  Y+D VAF  +I +LL RP G+ G+  
Sbjct: 231 IILGGMGNVKGAMAGGLLLGVAET-GIVAYGDSGYRDAVAFITIIFILLLRPQGLFGKKT 289

Query: 304 VE 305
            E
Sbjct: 290 AE 291


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: 317
Number of extensions: 17
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: 307
Length of database: 294
Length adjustment: 27
Effective length of query: 280
Effective length of database: 267
Effective search space:    74760
Effective search space used:    74760
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.

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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