GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacJ in Dinoroseobacter shibae DFL-12

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate 3609758 Dshi_3141 ABC transporter related (RefSeq)

Query= uniprot:D4GP38
         (383 letters)



>FitnessBrowser__Dino:3609758
          Length = 352

 Score =  306 bits (784), Expect = 6e-88
 Identities = 177/374 (47%), Positives = 236/374 (63%), Gaps = 39/374 (10%)

Query: 1   MGQIQLTDLTKRFGDTVAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGDI 60
           M ++ L DLTKR+GD V VD+ SL + DEEFLVL+GPSGCGK+TT+RM+AGLE PT G+I
Sbjct: 1   MAEVILKDLTKRWGDFVGVDNQSLHVRDEEFLVLLGPSGCGKTTTMRMIAGLEDPTDGEI 60

Query: 61  YIGGDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVAE 120
           +IG   +N  +P++RD+AMVFQ+Y LYPHMT+ +NI + L    G   AE   RV   AE
Sbjct: 61  WIGDRMVNDDLPKDRDVAMVFQNYGLYPHMTIFENIAYPLRVR-GVDKAEIPPRVQRAAE 119

Query: 121 TLGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQNL 180
            + +   L RKP  LSGGQ+QRVAL RAIVR P+VFLMDEPLSNLDAKLR  MR EL++L
Sbjct: 120 QVELTKFLHRKPKALSGGQRQRVALARAIVRKPKVFLMDEPLSNLDAKLRVTMRAELKHL 179

Query: 181 QDQLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPMI 240
             +L +TTVYVTH+Q EAMT+ADR+AVM  G +QQ+ +P E Y++P NLFVA FIG P +
Sbjct: 180 SRELQITTVYVTHDQIEAMTLADRVAVMKHGVIQQLGTPDEIYNDPANLFVAGFIGSPAM 239

Query: 241 NLVRGTRSESTFVGEHFSYPLDEDVMESVDDRDDFVLGVRPEDIEVADAAPDDAALDDHD 300
           NL+ G+  +  FV    +      V     DR   +LGVR +D++V +A   D       
Sbjct: 240 NLINGSVEDGMFVTTGGT----RLVKVPSPDRARAILGVRADDMQVHEAGQGD------- 288

Query: 301 LQMDVTV--VEPHGDQNVLHLSHPDQPSADDALQAVTEGMHLVTRGDR---------VTV 349
             +DVT+   E  G+  +L +    Q               ++ RGDR         V +
Sbjct: 289 --IDVTIYAFENTGESTLLTVQWGKQ--------------RVIARGDRHLRKEQDDVVGI 332

Query: 350 TIPPDKIHLFDAET 363
           ++  D ++LFD +T
Sbjct: 333 SLNTDHLYLFDPDT 346


Lambda     K      H
   0.317    0.135    0.386 

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: 434
Number of extensions: 17
Number of successful extensions: 2
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: 383
Length of database: 352
Length adjustment: 30
Effective length of query: 353
Effective length of database: 322
Effective search space:   113666
Effective search space used:   113666
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: 49 (23.5 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:

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