Alignments for a candidate for gguA in Collimonas pratensis Ter91

GapMind for catabolism of small carbon sources

Alignments for a candidate for gguA in Collimonas pratensis Ter91

Align GguA aka ATU2347 aka AGR_C_4264, component of Multiple sugar (arabinose, xylose, galactose, glucose, fucose) putative porter (characterized)
to candidate WP_099047275.1 CPter91_RS07335 sugar ABC transporter ATP-binding protein

Query= TCDB::O05176
         (512 letters)



>NCBI__GCF_001584185.1:WP_099047275.1
          Length = 510

 Score =  379 bits (973), Expect = e-109
 Identities = 218/514 (42%), Positives = 326/514 (63%), Gaps = 24/514 (4%)

Query: 6   LEMRNITKTFPGVKALENVNLKVKEGEIHALVGENGAGKSTLMKVLSGVYPAGTYEGEIH 65
           + + NITK FPGV AL+N    ++ GE+HAL+GENGAGKSTLMKVL+GVYP  +  GEI 
Sbjct: 1   MSLENITKRFPGVLALDNCRFDLQRGEVHALMGENGAGKSTLMKVLAGVYPKDS--GEIR 58

Query: 66  YEGAVRNFRAINDSEDIGIIIIHQELALVPLLSIAENIFLGNEVASN-GVISWQQTFNR- 123
             G +        ++ +GI IIHQEL L+  L+ A+NIF+G E     G+   +   NR 
Sbjct: 59  IAGQLVEIPTPRAAQALGIGIIHQELNLMNHLTAAQNIFIGREPRGRLGMFLDEDALNRK 118

Query: 124 TRELLKKVGLKESPETLITDIGVGKQQLVEIAKALSKSVKLLILDEPTASLNESDSEALL 183
           TRE+ +++ L   P TL++++ V KQQ+VEIAKALS   ++LI+DEPTA+LN ++ E L 
Sbjct: 119 TREIFERMRLDLDPATLVSELTVAKQQMVEIAKALSFDSRVLIMDEPTAALNNAEIEDLF 178

Query: 184 NLLMEFRNQGMTSIIITHKLNEVRKVADQITVLRDGMTVKTLDCHQEEISEDVIIRNMVG 243
            ++ + ++ G+  + I+HK++E+R++++++TV+RDG  + T+       S + II  MVG
Sbjct: 179 RIIRQLQSHGVGIVYISHKMDELRQISNRVTVMRDGQYIATVPT--ATTSMETIIGMMVG 236

Query: 244 RDLEDRYPPRDVPI---GETILEVKNWNAYHQQHRDRQVLHDINVTVRKGEVVGIAGLMG 300
           R +++  P  DVP     E +LEVK              + D+N T+RKGE++G AGLMG
Sbjct: 237 RQIDNSGP--DVPDTSGNEIVLEVKGLQR-------GAFIKDVNFTLRKGEILGFAGLMG 287

Query: 301 AGRTEFAMSVFGKSYGHRI-TGDVLIDGKPVDVSTVRKAIDAGLAYVTEDRKHLGLVLND 359
           AGRTE A +VFG     R+  G++L+ G  V + + + A+  G+ Y++EDRKH GL    
Sbjct: 288 AGRTEVARAVFGAD---RVDAGEILVHGARVSIRSPKDAVAHGIGYLSEDRKHFGLATGL 344

Query: 360 NILHNTTLANLAG-VSKASIIDDIKEMKVASDFRTRLRIRSSGIFQETVNLSGGNQQKVV 418
           ++  N  ++++   +++   +D       A  +  +L I++  + Q    LSGGNQQK+V
Sbjct: 345 DVKTNVAMSSMNQFLTQGLFLDQAAIRDTAQGYVRQLSIKTPSVDQPVRLLSGGNQQKIV 404

Query: 419 LSKWLFSNPDVLILDEPTRGIDVGAKYEIYTIINQLAADGKGVLMISSEMPELLGNCDRI 478
           ++KWL  + D+L  DEPTRGID+GAK EIY ++N LA  GK ++MISSE+PE+L    RI
Sbjct: 405 IAKWLLRDCDILFFDEPTRGIDIGAKSEIYKLLNSLAEQGKAIVMISSELPEVLRMSHRI 464

Query: 479 YVMNEGRIVAELPKGEASQESIMR-AIMRSGEKN 511
            VM EGRI  EL   EASQE IM+ A +R  +++
Sbjct: 465 LVMCEGRITGELSAAEASQEKIMQLATLREDKRD 498


Lambda     K      H
   0.316    0.135    0.374 

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: 597
Number of extensions: 23
Number of successful extensions: 9
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: 512
Length of database: 510
Length adjustment: 35
Effective length of query: 477
Effective length of database: 475
Effective search space:   226575
Effective search space used:   226575
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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Protein sequences (fasta format)
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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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

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:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 2024 update on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

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

GapMind for catabolism of small carbon sources