GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Streptococcus massiliensis 4401825

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_018371595.1 BN415_RS07285 branched-chain amino acid ABC transporter permease

Query= TCDB::P21627
         (307 letters)



>NCBI__GCF_000341525.1:WP_018371595.1
          Length = 289

 Score =  248 bits (634), Expect = 9e-71
 Identities = 131/301 (43%), Positives = 192/301 (63%), Gaps = 14/301 (4%)

Query: 8   LQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYIAFIAITLLAMMGLDS 67
           LQQLVNGL +GS YAL+A+GYTMVYGII +INFAHG++YM+G+++ +  I         S
Sbjct: 2   LQQLVNGLILGSVYALLALGYTMVYGIIKLINFAHGDIYMMGAFMGYYLI--------GS 53

Query: 68  VPLMMLAAFAASIIVTSAFGYSIERVAYRPLRGGNRLIPLISAIGMSIFLQNAVMLSQDS 127
           + +    A   S++ T+A G  IE +AYRPLR   R+  LI+AIG+S FL+ +++    +
Sbjct: 54  LHMNFYLALIVSMVGTAALGVLIEFLAYRPLRHSTRIAALITAIGVSFFLEYSMVAVVSA 113

Query: 128 KEKAIPTLLPG-NFVFGESSMNGVVISYMQILIFVVTFLVMFGLTLFISRSRLGRACRAC 186
             KA P +LP   FV G  S+  +     Q+ I  V  ++M  L L + ++++G+A RA 
Sbjct: 114 NVKAFPQVLPSVRFVLGPVSVTSI-----QLTILAVALILMVLLQLIVQKTKMGKAMRAV 168

Query: 187 AEDLKMTNLLGINSNNIIALTFVIGAALAAVAAVLLGMQYGVINPGIGFLAGIKAFTAAV 246
           + D     L+GIN N  I+ TF +G+ALA  A VL+ + Y  ++P +G   G+K+F AAV
Sbjct: 169 SVDSDAAQLMGINVNQTISFTFALGSALAGAAGVLIALYYNSLDPLMGMTPGLKSFVAAV 228

Query: 247 LGGIGSIPGAMLGGLLLGVAEAFGADVFGDQYKDVVAFGLLILVLLFRPTGILGRPEVEK 306
           +GGIG IPGA LGG ++G+ E F   +   +Y+D + +G+LIL+LL RP GILG+   EK
Sbjct: 229 IGGIGIIPGAALGGFVIGILETFATVINLSEYRDAIVYGILILILLIRPAGILGKNVKEK 288

Query: 307 V 307
           V
Sbjct: 289 V 289


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: 311
Number of extensions: 15
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: 289
Length adjustment: 26
Effective length of query: 281
Effective length of database: 263
Effective search space:    73903
Effective search space used:    73903
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