Align Iron-sulfur cluster-binding protein (characterized, see rationale)
to candidate WP_011386479.1 AMB_RS20890 iron-sulfur cluster-binding protein
Query= uniprot:Q726S3 (717 letters) >lcl|NCBI__GCF_000009985.1:WP_011386479.1 AMB_RS20890 iron-sulfur cluster-binding protein Length = 478 Score = 272 bits (696), Expect = 2e-77 Identities = 175/452 (38%), Positives = 234/452 (51%), Gaps = 21/452 (4%) Query: 24 RNAMDKFAVAYRASRANAFKDIDE-KAIIAEVADAKDHAAKNMDTLYAQFKAEAEKRGVK 82 R AMD RA F D E A+ A A A+ +A + L Q +A + G+ Sbjct: 28 RRAMD----GLMTKRAAQFADEAEWNALRARGAAARANALAKLPELLEQLEANCLRNGIH 83 Query: 83 VHLARTAAEANEIIARIARDNNCKKAIKSKSMTAEETHLNHRLEEDNVEVIETDLGEWII 142 VH A T AEAN I+ I + IK KSM EE HLN LE+ + +E+DLGE+II Sbjct: 84 VHWAETTAEANAIVLGILEAAGARTVIKGKSMVTEEMHLNAHLEKHGITPVESDLGEYII 143 Query: 143 QMRHEGPSHMVMPAIHLSRYQVADLFSE-VTKQKQEVDIQRLVKVARRELRTHFATADMG 201 Q+ E PSH+VMP IH ++ ++A+LF + + Q ++ L AR LR FA AD G Sbjct: 144 QLAGEAPSHIVMPCIHKNKTEIAELFHDKIEGQPYTENVDELTAAARAALRGAFAGADAG 203 Query: 202 ISGANFAVAETGTIGLVTNEGNARLVTTLPRVHVALAGLDKLVPTLHDALRSLKVLPRNA 261 ISG NFAVAETGT+ L+ NEGN RL TTLP +H+A+ G++K++ L D L +LPR+A Sbjct: 204 ISGVNFAVAETGTLVLIENEGNGRLSTTLPPLHIAVTGIEKVLEKLDDVPPLLSLLPRSA 263 Query: 262 TGQAITSYVTWIGGANECEACVDGRKEMHIVFLDNGRRALAEDPLFSQVLRCVRCGACAN 321 TGQ IT+YV I + E DG K +H+V LDNGR + D LRC+RC AC N Sbjct: 264 TGQPITTYVNMISSPRK-EGEKDGPKAVHLVLLDNGRSRVHGDTELRDTLRCIRCAACMN 322 Query: 322 VCPVYRLVGGHKMGHIYIGAIGLILTYFFHGRDKARNLVQNCINCESCKHICAGGIDLPR 381 CPVY VGGH Y G IG +LT G D A + C +C +C I +P Sbjct: 323 HCPVYTRVGGHTYTFTYPGPIGKLLTPQIEGLDCAGDQPHASTLCRACADVCPVQIPIPD 382 Query: 382 LIKEIRARLNEEEGMPVETTLMGKMLKNRKLFHTLLRFAKWAQKPVTGGTPYIRHLPQIF 441 L+ RL E P + G+ +K T W + +P + +I Sbjct: 383 LL----VRLRTESVRPTQ----GQAVKGAGSSATTSETLGWKGWTLLYASPLVY---RIG 431 Query: 442 AKDHGFKALPAIADKPFRDEWETVRPRIAKPK 473 K G+ + P +W +VR KPK Sbjct: 432 TKMLGWFGNLMPSSAPMLKQWTSVR---TKPK 460 Lambda K H 0.321 0.135 0.402 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: 767 Number of extensions: 42 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: 717 Length of database: 478 Length adjustment: 37 Effective length of query: 680 Effective length of database: 441 Effective search space: 299880 Effective search space used: 299880 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 (21.9 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.
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:
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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