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 |
Related structures:
AlphaFold database: Q4Q545
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.771 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.811 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.737 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.689 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.811 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.821 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.796 |
CLV_PCSK_PC1ET2_1 | 56 | 58 | PF00082 | 0.465 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.734 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.765 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.778 |
CLV_PCSK_SKI1_1 | 348 | 352 | PF00082 | 0.781 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.675 |
DEG_APCC_DBOX_1 | 163 | 171 | PF00400 | 0.546 |
DOC_CYCLIN_RxL_1 | 161 | 172 | PF00134 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.665 |
DOC_CYCLIN_yCln2_LP_2 | 415 | 421 | PF00134 | 0.765 |
DOC_MAPK_DCC_7 | 412 | 421 | PF00069 | 0.762 |
DOC_MAPK_gen_1 | 171 | 180 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 260 | 267 | PF00069 | 0.759 |
DOC_MAPK_gen_1 | 412 | 421 | PF00069 | 0.824 |
DOC_PP1_RVXF_1 | 261 | 268 | PF00149 | 0.816 |
DOC_PP2B_LxvP_1 | 415 | 418 | PF13499 | 0.722 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.580 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.824 |
DOC_WW_Pin1_4 | 254 | 259 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.823 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.823 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.523 |
LIG_14-3-3_CanoR_1 | 348 | 353 | PF00244 | 0.754 |
LIG_14-3-3_CanoR_1 | 363 | 371 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 439 | 443 | PF00244 | 0.842 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.597 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.572 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.811 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.653 |
LIG_FHA_2 | 447 | 453 | PF00498 | 0.734 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.627 |
LIG_LIR_Gen_1 | 270 | 281 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.662 |
LIG_NRBOX | 165 | 171 | PF00104 | 0.493 |
LIG_Pex14_2 | 337 | 341 | PF04695 | 0.566 |
LIG_Rb_LxCxE_1 | 42 | 59 | PF01857 | 0.539 |
LIG_SH2_CRK | 12 | 16 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 408 | 411 | PF00017 | 0.697 |
LIG_SH3_2 | 114 | 119 | PF14604 | 0.722 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.703 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.728 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.624 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.586 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.786 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.702 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.811 |
LIG_SUMO_SIM_par_1 | 166 | 172 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 417 | 423 | PF11976 | 0.769 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.671 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.685 |
LIG_UBA3_1 | 166 | 173 | PF00899 | 0.667 |
LIG_WW_1 | 405 | 408 | PF00397 | 0.641 |
LIG_WW_3 | 257 | 261 | PF00397 | 0.608 |
MOD_CDC14_SPxK_1 | 257 | 260 | PF00782 | 0.608 |
MOD_CDC14_SPxK_1 | 376 | 379 | PF00782 | 0.837 |
MOD_CDK_SPK_2 | 420 | 425 | PF00069 | 0.776 |
MOD_CDK_SPxK_1 | 254 | 260 | PF00069 | 0.612 |
MOD_CDK_SPxK_1 | 373 | 379 | PF00069 | 0.828 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.700 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.553 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.760 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.833 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.664 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.693 |
MOD_CK2_1 | 446 | 452 | PF00069 | 0.736 |
MOD_Cter_Amidation | 437 | 440 | PF01082 | 0.651 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.625 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.707 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.639 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.611 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.655 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.793 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.796 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.653 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.687 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.579 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.720 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.600 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.777 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.773 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.576 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.814 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.655 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.747 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.636 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.645 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.740 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.784 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.783 |
MOD_N-GLC_2 | 323 | 325 | PF02516 | 0.751 |
MOD_NEK2_2 | 339 | 344 | PF00069 | 0.829 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.587 |
MOD_PIKK_1 | 331 | 337 | PF00454 | 0.791 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.625 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.850 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.804 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.574 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.656 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.635 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.677 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.674 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.698 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.775 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.737 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.691 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.574 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.809 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.737 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.780 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.769 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.720 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.821 |
MOD_ProDKin_1 | 254 | 260 | PF00069 | 0.690 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.828 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.823 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.522 |
MOD_SUMO_for_1 | 55 | 58 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 255 | 265 | PF00179 | 0.806 |
TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.657 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.656 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.675 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ITE5 | Leishmania donovani | 85% | 100% |
A4HKM1 | Leishmania braziliensis | 63% | 100% |
A4I853 | Leishmania infantum | 85% | 100% |
E9B310 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |