GapMind for catabolism of small carbon sources

 

Alignments for a candidate for braD in Desulfuromusa kysingii DSM 7343

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_092349194.1 BLU87_RS12680 branched-chain amino acid ABC transporter permease

Query= TCDB::P21627
         (307 letters)



>NCBI__GCF_900107645.1:WP_092349194.1
          Length = 298

 Score =  250 bits (638), Expect = 3e-71
 Identities = 132/301 (43%), Positives = 196/301 (65%), Gaps = 6/301 (1%)

Query: 7   YLQQLVNGLTVGSTYALIAIGYTMVYGIIGMINFAHGEVYMIGSYIAFIAITLLAMMGLD 66
           +LQQL NGLT+GS +AL+A+GYTMVYG++ +INFAHG++    +++     T   ++G  
Sbjct: 4   FLQQLANGLTIGSMFALVALGYTMVYGVMKLINFAHGDMVAASAFVGLTIYT--QVLGQA 61

Query: 67  SVPLMMLAAFAASIIVTSAFGYSIERVAYRPLRGGNRLIPLISAIGMSIFLQNAVMLSQD 126
           +  + ++A F  S +V +  G  +ER+AYRPLR   RL  ++SA+G S+ +QN +ML   
Sbjct: 62  TSLIAVIAIFLLSAMVMACVGILLERLAYRPLREAPRLSAVVSALGASLVIQNGIMLIWG 121

Query: 127 SKEKAIPTLLPGNFVFGESSMNGVVISYMQILIFVVTFLVMFGLTLFISRSRLGRACRAC 186
            + +  P L+P  +      + GVVIS +Q+LI V + ++M  L LF+ ++R+G A RA 
Sbjct: 122 PQMRIFPELVPQVYW----DLGGVVISLIQVLILVFSLVLMIALYLFVEKTRMGAAIRAS 177

Query: 187 AEDLKMTNLLGINSNNIIALTFVIGAALAAVAAVLLGMQYGVINPGIGFLAGIKAFTAAV 246
           A D     L+GIN N++IAL F+IG++L AV  + +G+ Y  I   +G+  G+ AF AA+
Sbjct: 178 AIDQDAARLMGINVNSVIALIFIIGSSLGAVGGLFIGLYYRGITFNMGWQYGLYAFIAAI 237

Query: 247 LGGIGSIPGAMLGGLLLGVAEAFGADVFGDQYKDVVAFGLLILVLLFRPTGILGRPEVEK 306
           LGGIG+IPGAMLGG+LLG+ +AF A      + D   F LLIL+L+ RPTG+LG    EK
Sbjct: 238 LGGIGNIPGAMLGGMLLGLFQAFIAGYISSTWADAFTFILLILILIVRPTGLLGERVAEK 297

Query: 307 V 307
           V
Sbjct: 298 V 298


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: 313
Number of extensions: 14
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: 298
Length adjustment: 27
Effective length of query: 280
Effective length of database: 271
Effective search space:    75880
Effective search space used:    75880
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