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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031390 | Ctf18 RFC-like complex | 3 | 5 |
GO:0032991 | protein-containing complex | 1 | 5 |
GO:0140513 | nuclear protein-containing complex | 2 | 5 |
Related structures:
AlphaFold database: A4HSW0
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 5 |
GO:0007062 | sister chromatid cohesion | 3 | 5 |
GO:0007064 | mitotic sister chromatid cohesion | 4 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016043 | cellular component organization | 3 | 5 |
GO:0022402 | cell cycle process | 2 | 5 |
GO:0051276 | chromosome organization | 5 | 5 |
GO:0071840 | cellular component organization or biogenesis | 2 | 5 |
GO:1903047 | mitotic cell cycle process | 3 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 349 | 353 | PF00656 | 0.632 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.607 |
CLV_PCSK_FUR_1 | 44 | 48 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.231 |
CLV_PCSK_PC1ET2_1 | 338 | 340 | PF00082 | 0.711 |
CLV_PCSK_PC7_1 | 185 | 191 | PF00082 | 0.337 |
CLV_PCSK_PC7_1 | 204 | 210 | PF00082 | 0.362 |
CLV_PCSK_PC7_1 | 39 | 45 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.560 |
DEG_COP1_1 | 360 | 370 | PF00400 | 0.556 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.553 |
DEG_SCF_FBW7_1 | 268 | 275 | PF00400 | 0.516 |
DEG_SPOP_SBC_1 | 133 | 137 | PF00917 | 0.693 |
DEG_SPOP_SBC_1 | 75 | 79 | PF00917 | 0.627 |
DOC_MAPK_gen_1 | 169 | 176 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 189 | 195 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 208 | 214 | PF00069 | 0.231 |
DOC_MAPK_MEF2A_6 | 169 | 178 | PF00069 | 0.412 |
DOC_MAPK_RevD_3 | 176 | 190 | PF00069 | 0.337 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.462 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.369 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.623 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 144 | 149 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.281 |
LIG_Actin_WH2_2 | 15 | 32 | PF00022 | 0.510 |
LIG_AP2alpha_1 | 295 | 299 | PF02296 | 0.651 |
LIG_BRCT_BRCA1_1 | 390 | 394 | PF00533 | 0.436 |
LIG_CtBP_PxDLS_1 | 71 | 75 | PF00389 | 0.545 |
LIG_eIF4E_1 | 379 | 385 | PF01652 | 0.457 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.412 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.537 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.653 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.617 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.666 |
LIG_LIR_Apic_2 | 205 | 210 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 381 | 388 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.553 |
LIG_Pex14_2 | 207 | 211 | PF04695 | 0.412 |
LIG_Pex14_2 | 295 | 299 | PF04695 | 0.651 |
LIG_SH2_NCK_1 | 382 | 386 | PF00017 | 0.483 |
LIG_SH3_1 | 159 | 165 | PF00018 | 0.672 |
LIG_SH3_2 | 154 | 159 | PF14604 | 0.653 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.775 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.761 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.224 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.527 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.588 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.679 |
LIG_UBA3_1 | 15 | 21 | PF00899 | 0.564 |
MOD_CDC14_SPxK_1 | 156 | 159 | PF00782 | 0.656 |
MOD_CDK_SPK_2 | 153 | 158 | PF00069 | 0.652 |
MOD_CDK_SPxK_1 | 153 | 159 | PF00069 | 0.653 |
MOD_CDK_SPxK_1 | 215 | 221 | PF00069 | 0.412 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.679 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.632 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.412 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.677 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.731 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.738 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.663 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.649 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.579 |
MOD_DYRK1A_RPxSP_1 | 161 | 165 | PF00069 | 0.362 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.705 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.656 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.701 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.309 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.609 |
MOD_GlcNHglycan | 305 | 310 | PF01048 | 0.678 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.671 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.660 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.658 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.742 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.681 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.671 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.599 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.679 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.719 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.371 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.689 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.523 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.741 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.649 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.721 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.587 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.729 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.588 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.605 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.566 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.412 |
MOD_PKA_1 | 144 | 150 | PF00069 | 0.688 |
MOD_PKA_1 | 189 | 195 | PF00069 | 0.337 |
MOD_PKA_1 | 38 | 44 | PF00069 | 0.697 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.721 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.394 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.281 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.697 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.398 |
MOD_Plk_1 | 272 | 278 | PF00069 | 0.587 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.587 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.437 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.577 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.387 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.626 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.721 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.768 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.342 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.429 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.662 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.763 |
TRG_DiLeu_BaEn_1 | 240 | 245 | PF01217 | 0.662 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 143 | 145 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.722 |
TRG_ER_diArg_1 | 46 | 49 | PF00400 | 0.617 |
TRG_NLS_Bipartite_1 | 208 | 227 | PF00514 | 0.362 |
TRG_NLS_MonoExtC_3 | 222 | 227 | PF00514 | 0.574 |
TRG_NLS_MonoExtN_4 | 221 | 227 | PF00514 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 223 | 228 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WPI0 | Leishmania donovani | 97% | 99% |
A4H4N4 | Leishmania braziliensis | 63% | 94% |
E9AKU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QJ09 | Leishmania major | 89% | 100% |