GapMind for catabolism of small carbon sources

 

Alignments for a candidate for citA in Saccharomonospora marina XMU15

Align Citrate:H+ symporter (characterized)
to candidate WP_009154436.1 SACMADRAFT_RS13775 MHS family MFS transporter

Query= TCDB::P16482
         (444 letters)



>NCBI__GCF_000244955.1:WP_009154436.1
          Length = 446

 Score =  193 bits (490), Expect = 1e-53
 Identities = 121/377 (32%), Positives = 192/377 (50%), Gaps = 15/377 (3%)

Query: 36  GNFLEQFDFFLFGFYATYI-AHTFFPASSEFASLMMTFAVFGAGFLMRPIGAIVLGAYID 94
           G  +E +D+++FG  A  +    FFP  S  A  +  F+ F  GF+ RP+GA V+G + D
Sbjct: 22  GTSIEWYDYYIFGTAAALVFGSLFFPEFSATAGTLAAFSAFAVGFIARPLGAAVIGHFGD 81

Query: 95  KVGRRKGLIVTLSIMATGTFLIVLIPSYQTIGLWAPLLVLIGRLLQGFSAGAELGGVSVY 154
           ++GR+  L++TL +    TFLI ++P+Y  IGL AP+L+ + R+LQGF  G E GG  + 
Sbjct: 82  RIGRKSMLVLTLLLTGGTTFLIGVLPTYAAIGLAAPVLLTLLRVLQGFGVGGEWGGAVLI 141

Query: 155 LAEIATPGRKGFYTSWQSGSQQVAIMVAAAMGFALNAVLEPSAISDWGWRIPFLFGVLIV 214
             E A+P R+  Y S+      V ++  + + F   + +   A  D+GWRIPFLF +++V
Sbjct: 142 ATEHASPRRRAVYGSFAQFGVPVGVL-TSNLAFLSVSGMSDEAFLDYGWRIPFLFSIVLV 200

Query: 215 PFIFILRRKLEETQEFTARRHHLAMRQVFATLLANWQ---VVIAGMMMVAMTTTAFYLIT 271
               ++R +L +  EF   + H  + +V    L   Q   +V+A +  +A      Y + 
Sbjct: 201 VVGILVRSRLRDAPEFEKAKQHKDLAKVPIAELFRQQPRNLVLASLASIAPPAVG-YTVI 259

Query: 272 VYAPTFGKKVLMLSASDSLLVTLLVAISNFFWLP---VGGALSDRFGRRSVLIAMTLLAL 328
           VY  T+G  V   +  D   +  L+  S   W+    V   LSDRFG + V     L A+
Sbjct: 260 VYMLTYGTTV---AGFDRTTLLTLILTSTALWIATIVVSAILSDRFGAKRVFTIGALTAV 316

Query: 329 ATAWP-ALTMLANAPSFLMMLSVLLWLSFIYGMYNGAMIPALTEIMPAEVRVAGFSLAYS 387
              WP  L  L N    +  L   +  + + G+  GA     +EI P  VR +G S+ Y 
Sbjct: 317 --LWPLPLFALVNTGETMPALLAFVVAAIVQGIMAGAQGGLFSEIFPMRVRYSGISIGYQ 374

Query: 388 LATAVFGGFTPVISTAL 404
           +   + G  TP+++TAL
Sbjct: 375 MGGMLGGALTPIVATAL 391


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: 524
Number of extensions: 39
Number of successful extensions: 6
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: 446
Length adjustment: 32
Effective length of query: 412
Effective length of database: 414
Effective search space:   170568
Effective search space used:   170568
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