GapMind for catabolism of small carbon sources

 

Alignments for a candidate for xacJ in Rhodobacter viridis JA737

Align Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale)
to candidate WP_110804244.1 C8J30_RS03245 ABC transporter ATP-binding protein

Query= uniprot:D4GP38
         (383 letters)



>NCBI__GCF_003217355.1:WP_110804244.1
          Length = 332

 Score =  264 bits (675), Expect = 2e-75
 Identities = 158/365 (43%), Positives = 207/365 (56%), Gaps = 37/365 (10%)

Query: 1   MGQIQLTDLTKRFGDTVAVDDLSLDIDDEEFLVLVGPSGCGKSTTLRMLAGLETPTSGDI 60
           MG+I L  +TKRFGD   +  + L I D EF+V VGPSGCGKST LR++AGLE  + G I
Sbjct: 1   MGEIVLKGVTKRFGDVEVIPPIDLAIHDGEFVVFVGPSGCGKSTLLRLIAGLEDVSGGKI 60

Query: 61  YIGGDHMNYRVPQNRDIAMVFQDYALYPHMTVRQNIRFGLEEEEGYTSAERDERVVEVAE 120
            I G       P +R +AMVFQ YALYPHM+V++NI F L+  +    AE + +V   A+
Sbjct: 61  EIDGKDATETAPSDRGLAMVFQSYALYPHMSVKKNIAFPLKMAK-LPPAEIEAKVQAAAK 119

Query: 121 TLGIADLLDRKPDELSGGQQQRVALGRAIVRDPEVFLMDEPLSNLDAKLRAEMRTELQNL 180
            L ++  LDRKP +LSGGQ+QRVA+GRAIVR PE FL DEPLSNLDA LR  MR E+  L
Sbjct: 120 VLNLSAYLDRKPGQLSGGQRQRVAIGRAIVRSPEAFLFDEPLSNLDAALRVNMRLEISEL 179

Query: 181 QDQLAVTTVYVTHNQTEAMTMADRIAVMDDGELQQVASPFECYHEPNNLFVAEFIGEPMI 240
              L  T +YVTH+Q EAMTMAD+I V+  G ++QV SP E Y  P N FVA FIG P +
Sbjct: 180 HHTLKTTMIYVTHDQVEAMTMADKIVVLQAGRIEQVGSPLELYRTPRNRFVAGFIGSPKM 239

Query: 241 NLVRGTRSESTFVGEHFSYPLDEDVMESVDDRDDFVLGVRPEDIEVADAAPDDAALDDHD 300
           N + G  +E+   G H                    +G+RPE I ++          +  
Sbjct: 240 NFIEG--AEAAKHGAH-------------------AIGIRPEHIRISTT--------EGM 270

Query: 301 LQMDVTVVEPHGDQNVLHLSHPDQPSADDALQAVTEGMHL-VTRGDRVTVTIPPDKIHLF 359
            +  V V E  G    LH+      + +  L  V  G  + +  GD V ++    ++H F
Sbjct: 271 WKGTVGVSEHLGSDTFLHV------TTEHGLLNVRAGGEVDLHHGDSVFLSPDMAQLHRF 324

Query: 360 DAETG 364
           D E G
Sbjct: 325 DKEGG 329


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: 326
Number of extensions: 14
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: 332
Length adjustment: 29
Effective length of query: 354
Effective length of database: 303
Effective search space:   107262
Effective search space used:   107262
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 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