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: Q4QJ09
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_NRD_NRD_1 | 158 | 160 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.590 |
CLV_PCSK_FUR_1 | 44 | 48 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.756 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 208 | 210 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.756 |
CLV_PCSK_PC7_1 | 185 | 191 | PF00082 | 0.402 |
CLV_PCSK_PC7_1 | 204 | 210 | PF00082 | 0.229 |
CLV_PCSK_PC7_1 | 39 | 45 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.739 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.735 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.498 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.505 |
DEG_SPOP_SBC_1 | 133 | 137 | PF00917 | 0.715 |
DEG_SPOP_SBC_1 | 75 | 79 | PF00917 | 0.677 |
DOC_MAPK_gen_1 | 189 | 195 | PF00069 | 0.262 |
DOC_MAPK_gen_1 | 208 | 214 | PF00069 | 0.271 |
DOC_MAPK_MEF2A_6 | 169 | 178 | PF00069 | 0.453 |
DOC_MAPK_RevD_3 | 176 | 190 | PF00069 | 0.358 |
DOC_PP4_FxxP_1 | 207 | 210 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.796 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.615 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 105 | 113 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 144 | 149 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 376 | 383 | PF00244 | 0.454 |
LIG_Actin_WH2_2 | 15 | 32 | PF00022 | 0.552 |
LIG_AP2alpha_1 | 296 | 300 | PF02296 | 0.702 |
LIG_BIR_III_4 | 61 | 65 | PF00653 | 0.581 |
LIG_BRCT_BRCA1_1 | 391 | 395 | PF00533 | 0.382 |
LIG_eIF4E_1 | 380 | 386 | PF01652 | 0.410 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.335 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.554 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.583 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.674 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.740 |
LIG_LIR_Apic_2 | 205 | 210 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 382 | 389 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 378 | 383 | PF02991 | 0.497 |
LIG_Pex14_2 | 207 | 211 | PF04695 | 0.453 |
LIG_Pex14_2 | 296 | 300 | PF04695 | 0.702 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.598 |
LIG_SH3_1 | 159 | 165 | PF00018 | 0.683 |
LIG_SH3_2 | 154 | 159 | PF14604 | 0.660 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.571 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.744 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.760 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.211 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.655 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.789 |
LIG_SUMO_SIM_anti_2 | 112 | 118 | PF11976 | 0.559 |
LIG_UBA3_1 | 15 | 21 | PF00899 | 0.633 |
MOD_CDC14_SPxK_1 | 156 | 159 | PF00782 | 0.662 |
MOD_CDK_SPK_2 | 153 | 158 | PF00069 | 0.662 |
MOD_CDK_SPxK_1 | 153 | 159 | PF00069 | 0.662 |
MOD_CDK_SPxK_1 | 215 | 221 | PF00069 | 0.335 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.598 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.644 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.685 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.453 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.278 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.616 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.704 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.794 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.786 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.653 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.559 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.611 |
MOD_DYRK1A_RPxSP_1 | 161 | 165 | PF00069 | 0.679 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.646 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.603 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.668 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.718 |
MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.718 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.634 |
MOD_GlcNHglycan | 60 | 65 | PF01048 | 0.664 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.632 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.628 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.680 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.324 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.294 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.649 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.671 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.580 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.693 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.653 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.630 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.634 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.650 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.740 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.590 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.560 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.342 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.460 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.335 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.326 |
MOD_PKA_1 | 189 | 195 | PF00069 | 0.402 |
MOD_PKA_1 | 311 | 317 | PF00069 | 0.563 |
MOD_PKA_1 | 39 | 45 | PF00069 | 0.627 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.526 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.684 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.304 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.356 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.605 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.488 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.389 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.652 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.707 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.689 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.580 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.530 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.584 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.390 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.708 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.665 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.278 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.335 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.664 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.640 |
TRG_DiLeu_BaEn_1 | 240 | 245 | PF01217 | 0.669 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.416 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.335 |
TRG_ER_diArg_1 | 311 | 313 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 338 | 341 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 46 | 49 | PF00400 | 0.598 |
TRG_NLS_Bipartite_1 | 208 | 227 | PF00514 | 0.389 |
TRG_NLS_MonoExtC_3 | 222 | 227 | PF00514 | 0.453 |
TRG_NLS_MonoExtC_3 | 337 | 342 | PF00514 | 0.601 |
TRG_NLS_MonoExtN_4 | 221 | 227 | PF00514 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 223 | 228 | PF00026 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 236 | 240 | PF00026 | 0.541 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I714 | Leptomonas seymouri | 41% | 100% |
A0A3S7WPI0 | Leishmania donovani | 88% | 99% |
A4H4N4 | Leishmania braziliensis | 62% | 100% |
A4HSW0 | Leishmania infantum | 89% | 100% |
E9AKU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |