GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Desulfacinum infernum DSM 9756

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_073036690.1 BUB04_RS02685 branched-chain amino acid ABC transporter permease

Query= TCDB::P21627
         (307 letters)



>NCBI__GCF_900129305.1:WP_073036690.1
          Length = 297

 Score =  237 bits (605), Expect = 2e-67
 Identities = 132/302 (43%), Positives = 191/302 (63%), Gaps = 13/302 (4%)

Query: 7   YLQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYIAFIAITLLAMMGLD 66
           + QQL NG+++GS YAL+AIGYTMVYGI+ +INFAHG++ M+ +Y A  A+T+  +    
Sbjct: 6   FFQQLTNGISLGSLYALVAIGYTMVYGILRLINFAHGDLLMVAAYTAIYAVTMFTLPWYL 65

Query: 67  SVPLMMLAAFAASIIVTSAFGYSIERVAYRPLRGGNRLIPLISAIGMSIFLQNAVMLSQD 126
           S PL        +I +T   G  ++RVAY+PLR   R+  LISAIG S  L+N  ++   
Sbjct: 66  SFPL--------AIALTGCIGILLDRVAYKPLRDAPRISLLISAIGASFLLENLALVIIG 117

Query: 127 SKEKAIPTLLPGNFVFGESSMNGVVISYMQILIFVVTFLVMFGLTLFISRSRLGRACRAC 186
              K  P   P  F      + GV I  + I I ++T + +  L   + R+++G+A RA 
Sbjct: 118 GVPKGFPR--PDIFA-KVIEILGVRIQVLTIYIPLMTLVFLMALLYIVYRTKVGKAMRAA 174

Query: 187 AEDLKMTNLLGINSNNIIALTFVIGAALAAVAAVLLGMQYGVINPGIGFLAGIKAFTAAV 246
           ++D++ T L+GIN + IIALTF++G++LAA   ++  M+Y  +NP +G + G+KAF AAV
Sbjct: 175 SKDIETTRLMGINVDRIIALTFLMGSSLAAAGGIMWAMKYPQVNPFMGVIPGLKAFIAAV 234

Query: 247 LGGIGSIPGAMLGGLLLGVAEAFGADVFGD--QYKDVVAFGLLILVLLFRPTGILGRPEV 304
           LGGIG+I GA++GG  LG+ E      F    QY+D  AF +LILVLLFRPTGI+G P  
Sbjct: 235 LGGIGNIIGAVVGGFALGLGEILLVAFFPQLAQYRDAFAFVILILVLLFRPTGIMGEPIT 294

Query: 305 EK 306
           +K
Sbjct: 295 DK 296


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: 295
Number of extensions: 19
Number of successful extensions: 4
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: 297
Length adjustment: 27
Effective length of query: 280
Effective length of database: 270
Effective search space:    75600
Effective search space used:    75600
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 Apr 09 2024. 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