GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Aa in Rhodobacter viridis JA737

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_110804244.1 C8J30_RS03245 ABC transporter ATP-binding protein

Query= BRENDA::Q70HW1
         (384 letters)



>NCBI__GCF_003217355.1:WP_110804244.1
          Length = 332

 Score =  305 bits (782), Expect = 9e-88
 Identities = 172/364 (47%), Positives = 226/364 (62%), Gaps = 37/364 (10%)

Query: 1   MARVLLEHIYKTYPGQTEPTVKDFNLDIQDKEFTVFVGPSGCGKTTTLRMIAGLEDITEG 60
           M  ++L+ + K + G  E  +   +L I D EF VFVGPSGCGK+T LR+IAGLED++ G
Sbjct: 1   MGEIVLKGVTKRF-GDVE-VIPPIDLAIHDGEFVVFVGPSGCGKSTLLRLIAGLEDVSGG 58

Query: 61  NLYIGDRRVNDVPPKDRDIAMVFQNYALYPHMTVYQNMAFGLKLRKVPKAEIDRRVQEAA 120
            + I  +   +  P DR +AMVFQ+YALYPHM+V +N+AF LK+ K+P AEI+ +VQ AA
Sbjct: 59  KIEIDGKDATETAPSDRGLAMVFQSYALYPHMSVKKNIAFPLKMAKLPPAEIEAKVQAAA 118

Query: 121 KILDIAHLLDRKPKALSGGQRQRVALGRAIVREPQVFLMDEPLSNLDAKLRVQMRAEIRK 180
           K+L+++  LDRKP  LSGGQRQRVA+GRAIVR P+ FL DEPLSNLDA LRV MR EI +
Sbjct: 119 KVLNLSAYLDRKPGQLSGGQRQRVAIGRAIVRSPEAFLFDEPLSNLDAALRVNMRLEISE 178

Query: 181 LHQRLQTTVIYVTHDQTEAMTMGDRIVVMRDGVIQQADTPQVVYSQPKNMFVAGFIGSPA 240
           LH  L+TT+IYVTHDQ EAMTM D+IVV++ G I+Q  +P  +Y  P+N FVAGFIGSP 
Sbjct: 179 LHHTLKTTMIYVTHDQVEAMTMADKIVVLQAGRIEQVGSPLELYRTPRNRFVAGFIGSPK 238

Query: 241 MNFIRGEIVQDGDAFYFRAPSISLRLPEGRYGVLKASGAIGKPVVLGVRPEDLHDEEVFM 300
           MNFI G                             A  A      +G+RPE +       
Sbjct: 239 MNFIEG-----------------------------AEAAKHGAHAIGIRPEHIR----IS 265

Query: 301 TTYPDSVLQMQVEVVEHMGSEVYLHTSIGPNTIVARVNPRHVYHVGSSVKLAIDLNKIHI 360
           TT  + + +  V V EH+GS+ +LH +     +  R       H G SV L+ D+ ++H 
Sbjct: 266 TT--EGMWKGTVGVSEHLGSDTFLHVTTEHGLLNVRAGGEVDLHHGDSVFLSPDMAQLHR 323

Query: 361 FDAE 364
           FD E
Sbjct: 324 FDKE 327


Lambda     K      H
   0.321    0.138    0.395 

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: 384
Number of extensions: 21
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 384
Length of database: 332
Length adjustment: 29
Effective length of query: 355
Effective length of database: 303
Effective search space:   107565
Effective search space used:   107565
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 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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