GapMind for catabolism of small carbon sources

 

Alignments for a candidate for citA in Kocuria flava HO-9041

Align Citrate:H+ symporter (characterized)
to candidate WP_058857680.1 AS188_RS03520 MFS transporter

Query= TCDB::P16482
         (444 letters)



>NCBI__GCF_001482365.1:WP_058857680.1
          Length = 447

 Score =  242 bits (618), Expect = 2e-68
 Identities = 134/395 (33%), Positives = 215/395 (54%), Gaps = 3/395 (0%)

Query: 36  GNFLEQFDFFLFGFYATYIAHTFFPASSEFASLMMTFAVFGAGFLMRPIGAIVLGAYIDK 95
           GNF+E FD+ ++G+ A  IA  FFP S    +L+ TFA+F   F +RP+G  V G   DK
Sbjct: 40  GNFVEWFDYAIYGYLAATIAVVFFPESDPQTALLATFALFAISFFVRPLGGFVWGHLGDK 99

Query: 96  VGRRKGLIVTLSIMATGTFLIVLIPSYQTIGLWAPLLVLIGRLLQGFSAGAELGGVSVYL 155
           +GRR  L +++ IM+  TF I LIP Y TIG++AP+L+L+ R++QGFSA  E  G S +L
Sbjct: 100 LGRRTALSLSILIMSVSTFCIALIPGYATIGIFAPVLLLVVRIVQGFSAAGEYAGASAFL 159

Query: 156 AEIATPGRKGFYTSWQSGSQQVAIMVAAAMGFALNAVLEPSAISDWGWRIPFLFGVLIVP 215
            E A   R+G Y +    S    ++  +     L A+L    ++ WGWRIPFL    +  
Sbjct: 160 VEYAPANRRGLYAAVVPASTATGLLFGSLFVAGLTALLSDDQLNSWGWRIPFLLAAPMGL 219

Query: 216 FIFILRRKLEETQEF--TARRHHLAMRQVFATLLANWQVVIAGMMMVAMTTTAFYLITVY 273
               +R KLE+T  F   A    +    V      +W  ++  +  V +    FY++  Y
Sbjct: 220 IGRYIRTKLEDTPAFQELAEEDEVIQAPVRDMFRNHWGALLRAVGAVLLNAVGFYVLLSY 279

Query: 274 APTFGKKVLMLSASDSLLVTLLVAISNFFWLPVGGALSDRFGRRSVLIAMTLLALATAWP 333
            PT+  + + L  ++S L T L  +S   ++ + G  SDRFGR+ +L+A ++  +    P
Sbjct: 280 MPTYLSEEIGLGKTESFLATSLALLSYVGFIFLTGLASDRFGRKRMLMAASVSFVVLTVP 339

Query: 334 ALTMLANAPSFLMMLSVLLWLSFIYGMYNGAMIPALTEIMPAEVRVAGFSLAYSLATAVF 393
           A  M+  + +FL +L+V + L  +  + +G +   L E+ P  +R  GF+++++LA AVF
Sbjct: 340 AF-MVLESGTFLAVLAVQVLLGAMLTLNDGTLPSFLAELFPTRIRYTGFAVSFNLANAVF 398

Query: 394 GGFTPVISTALIEYTGDKASPGYWMSFAAICGLLA 428
           GG  P ++T LI       +P +++  AA    +A
Sbjct: 399 GGTAPFMATLLISAFATNLAPAWYLMAAAAVSFVA 433


Lambda     K      H
   0.329    0.139    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: 571
Number of extensions: 33
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: 444
Length of database: 447
Length adjustment: 32
Effective length of query: 412
Effective length of database: 415
Effective search space:   170980
Effective search space used:   170980
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 (21.9 bits)
S2: 51 (24.3 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