Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I0P0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 135 | 139 | PF00656 | 0.707 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.612 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 226 | 228 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.621 |
CLV_Separin_Metazoa | 8 | 12 | PF03568 | 0.565 |
DEG_APCC_DBOX_1 | 123 | 131 | PF00400 | 0.701 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.548 |
DOC_CYCLIN_RxL_1 | 33 | 45 | PF00134 | 0.680 |
DOC_SPAK_OSR1_1 | 198 | 202 | PF12202 | 0.636 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.724 |
DOC_USP7_UBL2_3 | 19 | 23 | PF12436 | 0.503 |
DOC_USP7_UBL2_3 | 222 | 226 | PF12436 | 0.654 |
LIG_14-3-3_CanoR_1 | 124 | 128 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 72 | 76 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 90 | 94 | PF00244 | 0.614 |
LIG_BIR_III_2 | 101 | 105 | PF00653 | 0.589 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.676 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.711 |
LIG_Integrin_RGD_1 | 186 | 188 | PF01839 | 0.803 |
LIG_SH2_SRC | 77 | 80 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.624 |
LIG_SH3_2 | 208 | 213 | PF14604 | 0.646 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.678 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.551 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.739 |
LIG_TRAF2_1 | 217 | 220 | PF00917 | 0.602 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.676 |
LIG_UBA3_1 | 9 | 14 | PF00899 | 0.506 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.679 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.634 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.611 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.694 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.633 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.694 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.723 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.578 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.601 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.660 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.672 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.705 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.588 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.606 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.613 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.707 |
MOD_N-GLC_2 | 192 | 194 | PF02516 | 0.547 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.471 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.538 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.679 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.493 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.780 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.607 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.668 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.693 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.555 |
TRG_DiLeu_BaEn_4 | 150 | 156 | PF01217 | 0.677 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.506 |
TRG_NLS_Bipartite_1 | 212 | 230 | PF00514 | 0.634 |
TRG_NLS_MonoCore_2 | 225 | 230 | PF00514 | 0.550 |
TRG_NLS_MonoExtC_3 | 225 | 231 | PF00514 | 0.587 |
TRG_Pf-PMV_PEXEL_1 | 212 | 216 | PF00026 | 0.634 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZZ3 | Leptomonas seymouri | 47% | 100% |
A0A3S7WYA2 | Leishmania donovani | 100% | 100% |
A4HDA7 | Leishmania braziliensis | 72% | 100% |
E9AWP0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QAT1 | Leishmania major | 86% | 98% |
V5C0P2 | Trypanosoma cruzi | 31% | 100% |