GapMind for catabolism of small carbon sources

 

Alignments for a candidate for bgl in Synechococcus elongatus PCC 7942

Align Beta-N-acetylglucosaminidase/beta-glucosidase; 3-beta-N-acetyl-D-glucosaminidase/beta-D-glucosidase; Nag3; EC 3.2.1.21; EC 3.2.1.52 (characterized)
to candidate Synpcc7942_0354 Synpcc7942_0354 Beta-glucosidase-related glycosidase-like

Query= SwissProt::Q7WUL3
         (564 letters)



>FitnessBrowser__SynE:Synpcc7942_0354
          Length = 542

 Score =  148 bits (373), Expect = 6e-40
 Identities = 110/346 (31%), Positives = 158/346 (45%), Gaps = 25/346 (7%)

Query: 55  LHVGGVMLRTMTAADAAATVTTLQSTATVPLLISANLEGGASQTVQEATHVGSNMALAAT 114
           L VGGV+L    AA+ A     LQ  + VPLLI+A++E G  Q    A      +AL+A 
Sbjct: 54  LGVGGVILLGGNAAEVALRCQQLQEWSRVPLLIAADIEEGVGQRFAGAVQFPPPLALSAI 113

Query: 115 GSTDH------VRRAATVIGREARALGINWAFTPVVDIDLNFRNPITNTRTFGADAATVA 168
            + D        R    +   EA A+ +NW   P+VDI+ N  NP+ N R FG D  TV+
Sbjct: 114 AAQDPERAQQLARSFGEITATEAIAIRLNWVLAPIVDINNNPANPVINVRAFGEDPETVS 173

Query: 169 AMGAEYVEAIQAQGLAASAKHFPGDGVDERDQHLLASVNTMSVEEWDDSFGVVYRAAIAA 228
            +   ++   Q   +  +AKHFPG G    D HL            +      +R AIAA
Sbjct: 174 QLTTAFIAGAQQFPVLTTAKHFPGHGDTATDSHLELPQIPHDRSRLEAVELEPFRRAIAA 233

Query: 229 GVKTVMVGHIMLPAYSRALRPGVADRDILPGVVAEELLNDLLRDRLGFNGLVVSDSTTMA 288
           GV  VM  H+ +PA          D D  P  ++  +L  LLR  LGF GL+V+D+  M 
Sbjct: 234 GVDAVMTAHLSIPA---------LDPD-YPATLSPAVLQGLLRRELGFEGLIVTDALVMQ 283

Query: 289 GLASVLPRSQAVPRVIAAGCDMFLFTKNLDEDFGYMRAGIRDGVITPERLDEAVTRILAL 348
            +A+     +A      AG D+ L   + +     +   IR+G IT +RL++++ RI   
Sbjct: 284 AIAAHYGPGEAARLAFEAGADILLMPVDPEAAIQEIAKAIREGQITYDRLEQSLARIWRA 343

Query: 349 K--------ASLGLHRGTNLPAQGA-AGVLADPDHSATAREVAASS 385
           K        AS   H     PA       ++ P H A A E+  +S
Sbjct: 344 KQKVCGARPASFLPHAWEQEPAIAIDLEAVSQPKHWAIAAEILTAS 389


Lambda     K      H
   0.318    0.134    0.391 

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: 649
Number of extensions: 31
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: 564
Length of database: 542
Length adjustment: 36
Effective length of query: 528
Effective length of database: 506
Effective search space:   267168
Effective search space used:   267168
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 53 (25.0 bits)

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

Links

Downloads

Related tools

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