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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031390 | Ctf18 RFC-like complex | 3 | 6 |
GO:0032991 | protein-containing complex | 1 | 6 |
GO:0140513 | nuclear protein-containing complex | 2 | 6 |
Related structures:
AlphaFold database: E9AKU8
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 6 |
GO:0007062 | sister chromatid cohesion | 3 | 6 |
GO:0007064 | mitotic sister chromatid cohesion | 4 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016043 | cellular component organization | 3 | 6 |
GO:0022402 | cell cycle process | 2 | 6 |
GO:0051276 | chromosome organization | 5 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 6 |
GO:1903047 | mitotic cell cycle process | 3 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.384 |
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.645 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.606 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.628 |
CLV_PCSK_FUR_1 | 44 | 48 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.215 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.704 |
CLV_PCSK_PC7_1 | 204 | 210 | PF00082 | 0.221 |
CLV_PCSK_PC7_1 | 39 | 45 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.639 |
DEG_COP1_1 | 362 | 372 | PF00400 | 0.536 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.471 |
DEG_SPOP_SBC_1 | 133 | 137 | PF00917 | 0.671 |
DEG_SPOP_SBC_1 | 75 | 79 | PF00917 | 0.639 |
DOC_MAPK_gen_1 | 169 | 176 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 208 | 214 | PF00069 | 0.215 |
DOC_MAPK_MEF2A_6 | 169 | 178 | PF00069 | 0.395 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.395 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.685 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.315 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 105 | 113 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.335 |
LIG_AP2alpha_1 | 297 | 301 | PF02296 | 0.651 |
LIG_BIR_III_4 | 61 | 65 | PF00653 | 0.585 |
LIG_BRCT_BRCA1_1 | 392 | 396 | PF00533 | 0.360 |
LIG_eIF4E_1 | 381 | 387 | PF01652 | 0.421 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.330 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.547 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.495 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.529 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.644 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.633 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.658 |
LIG_LIR_Apic_2 | 205 | 210 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 383 | 390 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 379 | 384 | PF02991 | 0.464 |
LIG_Pex14_2 | 207 | 211 | PF04695 | 0.395 |
LIG_Pex14_2 | 297 | 301 | PF04695 | 0.651 |
LIG_SH2_NCK_1 | 384 | 388 | PF00017 | 0.410 |
LIG_SH3_1 | 159 | 165 | PF00018 | 0.651 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.754 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.275 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.507 |
LIG_SH3_3 | 258 | 264 | PF00018 | 0.701 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.735 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.657 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.480 |
LIG_UBA3_1 | 15 | 21 | PF00899 | 0.544 |
MOD_CDK_SPxK_1 | 215 | 221 | PF00069 | 0.315 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.474 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.620 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.706 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.692 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.634 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.702 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.705 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.637 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.508 |
MOD_DYRK1A_RPxSP_1 | 161 | 165 | PF00069 | 0.345 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.630 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.612 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.671 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.311 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.691 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.458 |
MOD_GlcNHglycan | 306 | 312 | PF01048 | 0.611 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.611 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.669 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.708 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.662 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.635 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.652 |
MOD_GlcNHglycan | 60 | 65 | PF01048 | 0.640 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.547 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.700 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.647 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.677 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.774 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.318 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.601 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.630 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.646 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.637 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.635 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.720 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.608 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.639 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.727 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.484 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.315 |
MOD_PKA_1 | 46 | 52 | PF00069 | 0.606 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.490 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.654 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.339 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.341 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.676 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.670 |
MOD_PKB_1 | 44 | 52 | PF00069 | 0.488 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.644 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.600 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.699 |
MOD_Plk_4 | 376 | 382 | PF00069 | 0.611 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.376 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.332 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.315 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.696 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.641 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.513 |
TRG_DiLeu_BaEn_1 | 240 | 245 | PF01217 | 0.635 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 45 | 47 | PF00400 | 0.639 |
TRG_NLS_Bipartite_1 | 208 | 227 | PF00514 | 0.345 |
TRG_NLS_MonoExtC_3 | 222 | 227 | PF00514 | 0.395 |
TRG_NLS_MonoExtC_3 | 338 | 343 | PF00514 | 0.579 |
TRG_NLS_MonoExtN_4 | 221 | 227 | PF00514 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 223 | 228 | PF00026 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I714 | Leptomonas seymouri | 40% | 100% |
A0A3S7WPI0 | Leishmania donovani | 83% | 100% |
A4H4N4 | Leishmania braziliensis | 60% | 94% |
A4HSW0 | Leishmania infantum | 84% | 100% |
Q4QJ09 | Leishmania major | 84% | 100% |