GapMind for catabolism of small carbon sources

 

Aligments for a candidate for braD in Cupriavidus basilensis 4G11

Align Transmembrane component of a broad range amino acid ABC transporter (characterized, see rationale)
to candidate RR42_RS16975 RR42_RS16975 ABC transporter permease

Query= uniprot:Q1MCU0
         (300 letters)



>FitnessBrowser__Cup4G11:RR42_RS16975
          Length = 311

 Score =  275 bits (703), Expect = 1e-78
 Identities = 151/310 (48%), Positives = 207/310 (66%), Gaps = 11/310 (3%)

Query: 1   MEYFVQQLLNGLTLGSIYGLVAIGYTMVYGIIGMINFAHGDIFMLGGFAALIVFLVLTSI 60
           M+ F+QQ++NGL LGSIY L+A+GYTMVYGI+G+INFAHGD+ M+G   AL   L L   
Sbjct: 1   MDIFIQQIVNGLVLGSIYALIALGYTMVYGILGIINFAHGDVLMIGALTALSAILGLQKF 60

Query: 61  FAGLPVAVLLLVMLVVAMLMTSLWNWTIERVAYRPLRGSFRLAPLITAIGMSITLSNFIQ 120
           F GLP  + L++  ++AM + +   +TIERVAYRPLR + RLAPLITAIG+SI L     
Sbjct: 61  FPGLPEWLTLVIATLIAMPVCAALAYTIERVAYRPLRNAPRLAPLITAIGVSIILQTLAM 120

Query: 121 VTQGPRNKPIPPMV-SSVYQFGNISVSL--KQIIIIVITAVLLTIFWYIVNRTALGRAQR 177
           +         P ++ SS    G+   ++  K+I+II +  +++     +VNRT LGRA R
Sbjct: 121 MIWSRNPLTFPQLLPSSPIDIGSTGATITGKEIVIIGMALMVMAGLLTLVNRTKLGRAMR 180

Query: 178 ATEQDRKMAALLGVNVDQTISITFVMGAALAAVAGTMYLMYYGVASFNDGFTPGVKAFTA 237
           AT +++K+A L+GVN +  IS TF++GAALAA+AG M    YG A F  GF PG+KAFTA
Sbjct: 181 ATAENQKVAGLMGVNPNFVISATFMIGAALAALAGVMMATNYGNAHFYMGFIPGLKAFTA 240

Query: 238 AVLGGIGSLPGAVFGGLLIGLIESLWSAY--------FTIAYKDVATFAILAFVLIFKPT 289
           AVLGGIG+L GA+ GG+L+GLIE+L + Y        F   Y+DV  F +L  VL+F+P+
Sbjct: 241 AVLGGIGNLAGAMVGGMLLGLIEALGAGYIGDLTNGVFGSNYQDVFAFIVLIIVLVFRPS 300

Query: 290 GILGRPEVEK 299
           GI+G    E+
Sbjct: 301 GIMGERVSER 310


Lambda     K      H
   0.329    0.143    0.421 

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: 356
Number of extensions: 17
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: 300
Length of database: 311
Length adjustment: 27
Effective length of query: 273
Effective length of database: 284
Effective search space:    77532
Effective search space used:    77532
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 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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